Catalytic Carbonylative Double Cyclization Reactions: Comparison
Please note this is a comparison between Version 2 by Dean Liu and Version 3 by Dean Liu.

Some examples of carbonylative double cyclization processes, which allow the one-step synthesis of complex molecular architectures from simple building blocks using the simplest and readily available C-1 unit (CO), are illustrated and discussed.

  • carbonylation
  • cyclization
  • double cyclization
  • fused heterocycles

1. Introduction

The importance of carbon monoxide as a C-1 unit in organic synthesis can hardly be overemphasized [1]. It is a readily available feedstock that can be easily obtained by steam reforming of light hydrocarbons (including natural gas), partial oxidation of petroleum hydrocarbons, or gasification of coal to give syngas (CO and H2) [2]. It can be installed into an organic substrate, usually under catalytic conditions, leading to the direct formation of high value-added carbonylated compounds with 100% atom economy (carbonylation reactions) [1].
Here, some examples of carbonylative double cyclization processes for the synthesis of carbonylated fused heterocycles (in particular, starting from suitably functionalized olefinic substrates) are presented.

2. Functionalized Olefinic Substrates

It is well-know that palladium(II)-based catalysts activate unsaturated carbon–carbon bonds towards the attack of a variety of nucleophilic groups (mainly oxygen- or nitrogen-based). The intramolecular version of this reactivity is of particular importance as it allows the construction of heterocyclic derivatives in a straightforward manner and under mild reaction conditions (Pd(II)-catalyzed heterocyclization reactions) [3]. On the other hand, it is also very well known that Pd(II) catalysts promote many important kinds of carbonylation processes, particularly under oxidative conditions, including cyclization processes in which carbon monoxide is inserted as a carbonyl function inside the newly formed ring (cyclocarbonylation reactions) [4]. It is therefore not surprising that several important methods have been developed in which a single Pd(II)-based catalytic system promotes, in one synthetic step, the sequential heterocyclization−cyclocarbonylation of suitably functionalized olefinic substrates that carry two nucleophilic moieties placed in appropriate positions to undergo double cyclization. Pioneering studies on this kind of reactivity were conducted by the Semmelhack and Yoshida research groups during the 1980s. In 1984, Semmelhack et al. reported the Pd(II)-promoted stereoselective carbonylative double cyclization of 1-(2-(hydroxymethyl)phenyl)prop-2-en-1-ols to give 3,3a,5,9b-tetrahydro-2H-furo[3,2-c]isochromen-2-ones with a cis junction between the newly formed rings using a stoichiometric amount of Pd(OAc)2 [5]. The process started with the intramolecular 6-exo-trig nucleophilic attack of the benzylic hydroxyl group to the double bond, activated by coordination to the Pd(II) center. This led to the formation of a cis-type alkylpalladium intermediate stabilized by chelation of the second hydroxyl group. The final bicyclic product was then formed through CO migratory insertion followed by intramolecular nucleophilic displacement by the hydroxyl, possibly via the formation of a palladacycle followed by reductive elimination (Scheme 1).
Scheme 1. Synthesis of 3,3a,5,9b-tetrahydro-2H-furo[3,2-c]isochromen-2-ones from 1-(2-(hydroxymethyl)phenyl)prop-2-en-1-ols [5].
Interestingly, when an oxidant for Pd(0) such as CuCl2 was employed to make the process catalytic, the reaction led to the formation of (E)-(2-(3-chloroprop-1-en-1-yl)phenyl)methanol from allylic chlorination (74% yield) [5]. Later on, however, suitable conditions were elaborated by the Yoshida group for performing the carbonylative double cyclization of 3-hydroxy-4-pentenoic acids to stereoselectively give tetrahydrofuro[3,2-b]furan-2,5-diones with a cis junction between the rings under Pd(II) catalysis (10 mol% PdCl2 in the presence of 3 equiv of CuCl2 and 3 equiv of AcONa, in glacial acetic acid as the solvent, at room temperature and under 1 atm of CO) (Scheme 2) [6]. The process took place through 5-exo-trig cyclization by the intramolecular nucleophilic attack of the carboxylic group to the double bond coordinated to the metal center, stabilized by hydroxyl chelation, to give a cis-type alkylpalladium complex followed by CO insertion and intramolecular nucleophilic displacement, possibly via the formation of a palladacycle followed by reductive elimination (Scheme 2) [6].
Scheme 2. Synthesis of tetrahydrofuro[3,2-b]furan-2,5-diones from 3-hydroxy-4-pentenoic acids [6].
The same research group then published the carbonylative double cyclization of 4-ene-1,3-diols under similar reaction conditions to obtain tetrahydrofuro[3,2-b]furan-2(3H)-ones (Scheme 3) [7].
Scheme 3. Synthesis of tetrahydrofuro[3,2-b]furan-2(3H)-ones from 4-ene-1,3-diols [7].
Considering that the bicyclic tetrahydrofuro[3,2-b]furan-2(3H)-one substructure is largely found in natural and biologically active molecules, the methods disclosed by Semmelhack and Yoshida for constructing this important core by the carbonylative double cyclization of enediol derivatives have been largely employed as the key step in the semi- or total synthesis of natural products and bioactive compounds. Representative examples are shown in Table 1.
Table 1. Representative examples of the Pd(II)-promoted carbonylative double cyclization of enediol derivatives in the synthesis of natural and bioactive products.
Entry Conditions Substrate Product Yield (%) Refs.
1 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 41 h Catalysts 13 01025 i001 Catalysts 13 01025 i002 63 [8]
2 PdCl2(MeCN)2, (10 mol%), CuCl2 (2.4 equiv), CO (1 atm), THF, 25 °C, 24 h Catalysts 13 01025 i003 Catalysts 13 01025 i004 65 [9]
3 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 8 h Catalysts 13 01025 i005 Catalysts 13 01025 i006 85 [10]
4 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (4 equiv), CO (1 atm), AcOH, 25 °C, 24 h Catalysts 13 01025 i007 Catalysts 13 01025 i008 93 [11]
5 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 33 h Catalysts 13 01025 i009 Catalysts 13 01025 i010 38 [12]
6 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 15 h Catalysts 13 01025 i011 Catalysts 13 01025 i012 >80 [13]
7 Pd(OAc)2 (1.5 equiv), CO

(1.1 atm), THF, 23 °C, 4 h
Catalysts 13 01025 i013 Catalysts 13 01025 i014 87 [14]
8 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 15 h Catalysts 13 01025 i015 Catalysts 13 01025 i016 81 [15]
9 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C Catalysts 13 01025 i017 Catalysts 13 01025 i018 63 [16]
10 PdCl2, CuCl, AcONa, CO, AcOH Catalysts 13 01025 i019 Catalysts 13 01025 i020 33 [17]
11 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 10 h Catalysts 13 01025 i021 Catalysts 13 01025 i022 85 [18]
12 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 23 °C, 24 h Catalysts 13 01025 i023 Catalysts 13 01025 i024 75 [19]
13 Pd(OAc)2 (1.5 equiv),

N-methylmorpholine (3 equiv), CO, THF, 25 °C, 15 h
Catalysts 13 01025 i025 Catalysts 13 01025 i026 58 [20]
14 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 20 h Catalysts 13 01025 i027 Catalysts 13 01025 i028 65 [21]
15 Pd(OAc)2 (10 mol%), CuCl2

(3 equiv), AcONa (3 equiv),

CO (1 atm), AcOH, 25 °C, 15 h
Catalysts 13 01025 i029 Catalysts 13 01025 i030 63, 70 [22][23]
16 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 24 h Catalysts 13 01025 i031 Catalysts 13 01025 i032 33 [24]
17 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 24 h Catalysts 13 01025 i033 Catalysts 13 01025 i034 87 [25]
18 PdCl2 (10 mol%), CuCl2 (3 equiv), AcONa (3 equiv), CO (1 atm), AcOH, 25 °C, 12 h Catalysts 13 01025 i035 Catalysts 13 01025 i036 61 [26]
19 PdCl2(MeCN)2 (10 mol%), CuCl2 (5 equiv), AcOLi (5 equiv), [Fe(CO)5] (0.5 equiv), AcOH, 60 °C, 1 h Catalysts 13 01025 i037 Catalysts 13 01025 i038 47 [27]
20 PdCl2(MeCN)2 (10 mol%), Cu(OAc)2 (4 equiv), LiCl

(4 equiv), [Fe(CO)5] (0.25 equiv), AcOH, 60 °C, 15 min
Catalysts 13 01025 i039 Catalysts 13 01025 i040 67 [28]
21 PdCl2(MeCN)2 (10 mol%), CuCl2 (4 equiv), AcOLi (4 equiv), [Fe(CO)5] (0.3 equiv), AcOH, 60 °C, 30 min Catalysts 13 01025 i041 Catalysts 13 01025 i042 75 [29]
Interestingly, using the appropriate enantiopure ligand, a kinetic resolution of (±)-pent-4-ene-1,3-diols was possible with the formation of the corresponding bicyclic lactone in noracemic form. This was exemplified by the Pd(OAc)2-catalyzed carbonylation of (±)-pent-4-ene-1,3-diol performed in the presence of an enantiopure bis(oxazoline) ligand and p-benzoquinone as an external oxidant to give (3aR,6aR)-tetrahydrofuro[3,2-b]furan-2(3H)-one in 29% yield and 62% ee (Scheme 4) [30].
Scheme 4. Kinetic resolution of (±)-pent-4-ene-1,3-diol leading to enantioenriched (3aR,6aR)-tetrahydrofuro[3,2-b]furan-2(3H)-one [30].
More recently, the kinetic resolution of (±)-pent-4-ene-1,3-diols to give nonracemic tetrahydrofuro[3,2-b]furan-2(3H)-ones [2-(S,S) up to 80% ee, 2-(R,R) up to 57% ee] has been realized under similar conditions [4 mol% of Pd(OAc)2, 12 mol% of 2,6-bis[(4R)-4-phenyl-2-oxazolinyl]pyridine as enantiopure ligand, 0.5 equiv of p-benzoquinone, and 10 equiv AcOH] using an ionic liquid as the solvent (such as 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, [Bmim][NTf2], 10 equiv), as shown in SchemeScheme 5 5 [31].
Scheme 5. Kinetic resolution of (±)-pent-4-ene-1,3-diol in [bmim][NTf2] leading to enantioenriched (3aS,6aS)-tetrahydrofuro[3,2-b]furan-2(3H)-one [31].
Interestingly, the Gracza group reported that the use of iron pentacarbonyl as an in situ liquid CO source may lead to improved results (significantly shorter reaction times, in particular) in the Pd(II)-catalyzed carbonylative double cyclization of enediols with a terminal double bond, as shown in SchemeScheme 6 6 [27][32][33].
Scheme 6. Carbonylative double cyclization of pent-4-ene-1,3-diol using [Fe(CO)5] as in situ CO source [32].
The same research group recently reported their reaction under flow conditions using a continuous microflow system, as shown in Scheme 7 [29][34].
Scheme 7. Carbonylative double cyclization of 4-ene-1,3-diols using [Fe(CO)5] as in situ CO source under flow conditions [34].
The carbonylative double cyclization process of enediols has also been reported to occur with 4-ene-1,2-diol derivatives. In this case, after the initial 5-exo-trig O-cyclization, in the cyclocarbonylation it is the free hydroxyl at C-2 that acts as internal nucleophile, with the formation of a 6-membered ring. This is illustrated by the formation of 8-((tert-butyldimethylsilyl)oxy)-2,6-dioxabicyclo[3.2.1]octan-3-one from 3-((tert-butyldimethylsilyl)oxy)pent-4-ene-1,2-diol, as shown in SchemeScheme 8 8 [35].
Scheme 8. 5-exo-trig O-cyclization followed by cyclocarbonylation with 6-membered ring closure [35].
The nucleophilic group undergoing initial heterocyclization can also be nitrogen-based. Thus, as early as 1985 the Tamaru and Yoshida group found that the Pd(II)-catalyzed carbonylative double cyclization of the N-protected 5-aminopent-1-en-3-ols yielded N-protected 6-hydroxyhexahydro-2H-furo[3,2-b]pyrrol-2-ones, using the same conditions employed for 4-penten-1,3-diols [36]. Among the protective groups tested, the –CO2Me group turned out as the most suitable, as exemplified in Scheme 9 [37].
Scheme 9. Formation of 6-hydroxyhexahydro-2H-furo[3,2-b]pyrrol-2-one derivatives from N-protected 5-aminopent-1-en-3-ols [37].
As predicted, owing to the higher degrees of freedom of the alkyl chain, N-protected 6-aminohex-1-en-3-ols were significantly less reactive, and relatively good results were usually observed with P = CONHPh, as shown in SchemeScheme 10 10 [37].
Scheme 10. Synthesis of 2-oxo-N-phenylhexahydrofuro[3,2-b]pyridine-4(2H)-carboxamide from 1-(4-hydroxyhex-5-en-1-yl)-3-phenylurea [37].
Later on, Jäger et al. reported the carbonylation of benzyl ((2R,3S)-2,3-dihydroxypent-4-en-1-yl)carbamate (Scheme 11a) as a key step in the synthesis of novel 1,4-iminoglycitol derivatives as potential glycosidase inhibitors [38]. On the other hand, the PdCl2-catalyzed carbonylation of benzyl ((2S,3S)-2,3-dihydroxypent-4-en-1-yl)carbamate gave benzyl (3aR,6S,6aS)-6-hydroxy-2-oxohexahydro-4H-furo[3,2-b]pyrrole-4-carboxylate in a 14% yield (Scheme 11b) [39].
Scheme 11. Synthesis of (a) benzyl (3aR,6R,6aS)-6-hydroxy-2-oxohexahydro-4H-furo[3,2-b]pyrrole-4-carboxylate (a precursor for the formation of glycosidase inhibitor derivatives) [38] and (b) benzyl (3aR,6S,6aS)-6-hydroxy-2-oxohexahydro-4H-furo[3,2-b]pyrrole-4-carboxylate [39].
Kinetic resolution of N-protected 5-aminopent-1-en-3-ols in the Pd(II)-catalyzed carbonylative double cyclization has been reported by Gracza et al. Thus, using enantiopure bisoxazoline ligands, nonracemic hexahydro-2H-furo[3,2-b]pyrrol-2-ones could be obtained as in SchemeScheme 12 12 [40].
Scheme 12. Kinetic resolution of (±)-N-(3-hydroxypent-4-en-1-yl)-4-methylbenzenesulfonamide leading to enantioenriched (3aR,6aR)-4-tosylhexahydro-2H-furo[3,2-b]pyrrol-2-one [40].
The gaseous CO-free conditions elaborated by the Gracza group for the carbonylation of 4-ene-1,3-diols, involving the use of liquid [Fe(CO)5] as an in situ CO source (Scheme 6), have also been successfully employed by the same research team in the Pd(II)-catalyzed carboylative double cyclization of N-protected 5-aminopent-1-en-3-ols, as in SchemeScheme 13 13 [32].
Scheme 13. Carbonylative double cyclization of tert-butyl (3-hydroxypent-4-en-1-yl)carbamate using [Fe(CO)5] as in situ CO source [32].
An interesting carbonylative double cyclization process has recently been developed by the Li group [41]. It involved the reaction of N-(2-aminoethyl)pent-4-enamide or N-(2-hydroxyethyl)pent-4-enamide derivatives with CO (1 atm) in the presence of PdCl2 as a catalyst (1 mol%) and p-benzoquinone as an oxidant (1.2 equiv) (Scheme 14). As shown in Scheme 14, the initial 5-exo-trig N-cyclization was followed by CO insertion and intramolecular nucleophilic displacement via the formation of an 8-membered ring palladacycle followed by reduction elimination [41].
Scheme 14. Carbonylative double cyclization of N-(2-aminoethyl)pent-4-enamide and N-(2-hydroxyethyl)pent-4-enamide derivatives [41].
A general approach leading to carbonylative double cyclization is the intramolecular Pauson–Khand reaction starting from suitable diene or enyne substrates. Since several excellent reviews have been published on this reaction [42][43][44], even in the most recent literature [45][46][47], this process will not be treated here; however, a particularly striking example in Scheme 15 gives the reader an idea of the powerfulness of this synthetic method for constructing complex carbonylated polycyclic compounds [48].
Scheme 15. Synthesis of 2a-(ethoxycarbonyl)-8-oxododecahydropentaleno[1,6-cd]pentalene-1-carboxylic acid from ethyl 5-acetoxy-1-(but-3-en-1-yl)-2,3,4,5-tetrahydropentalene-3a(1H)-carboxylate by Pauson–Khand-type intramolecular reaction [48].


  1. Gabriele, B. (Ed.) Carbon Monoxide in Organic Synthesis—Carbonylation Chemistry; Wiley-VCH: Weinheim, Germany, 2022.
  2. Reimert, R.; Marschner, F.; Renner, H.-J.; Boll, W.; Supp, E.; Brejc, M.; Liebner, W.; Schaub, G. Gas production, 2. In Ullmann’s Encyclopedia of Industrial Chemistry; Baltes, H., Göpel, W., Hesse, J., Eds.; Wiley-VCH: Weinheim, Germany, 2011; pp. 423–479.
  3. Li, J.J.; Gribble, G. (Eds.) Palladium in Heterocyclic Chemistry—A Guide for the Synthetic Chemist, 2nd ed.; Elsevier: Amsterdam, The Netherlands, 2006.
  4. Gabriele, B.; Della Ca’, N.; Mancuso, R.; Veltri, L.; Ziccarelli, I. Palladium(II)-Catalyzed Carbonylations. In Carbon Monoxide in Organic Synthesis—Carbonylation Chemistry; Gabriele, B., Ed.; Wiley-VCH: Weinheim, Germany, 2022; Chapter 7.
  5. Semmelhack, M.F.; Bodurow, C.; Baum, M. Direct Synthesis of Pyran-Lactones Related to Nafhthoquinone Antibiotics. Tetrahadron Lett. 1984, 25, 3171–3174.
  6. Tamaru, H.; Higashimura, K.; Hojo, M.; Yoshida, Z. PdII-Catalyzed Stereoselective Bis-Lactonization. Angew. Chem. Int. Ed. 1985, 24, 1045–1046.
  7. Tamaru, H.; Kobayashi, T.; Kawamura, S.; Hojo, M.; Yoshida, Z. Palladium Catalyzed Oxycarbonylation of 4-Penten-1,3-diols: Efficient Stereoselective Synthesis of cis 3-Hydroxytetrahydrofuran 2-Acetic Acid Lactones. Tetrahedron Lett. 1985, 26, 3207–3210.
  8. Gracza, T.; Hasenöhrl, T.; Stahl, T.; Jäger, V. Synthesis of 3,5-Anhydro-2-deoxy-1,4-glyconolactones by Palladium(II)-Catalyzed, Regioselective Oxycarbonylation of C5- and C6-enitols. ω-Homologation of Aldoses to Produce Intermediates for C-Glycoside/C-Nucleoside Synthesis. Synthesis 1991, 1991, 1108–1118.
  9. Kraus, G.A.; Li, J. Regiocontrol by Remote Substituents. An Enantioselective Total Synthesis of Frenolicin B via a Highly Regioselective Diels-Alder Reaction. J. Am. Chem. Soc. 1993, 115, 5859–5860.
  10. Gracza, T.; Jäger, V. Synthesis of Natural and Unnatural Enantiomers of Goniofufurone and Its 7-Epimers from D-Glucose. Application of Palladium(II)—Catalyzed Oxycarbonylation of Unsaturated Polyols. Synthesis 1994, 1994, 1359–1368.
  11. Boukouvalas, J.; Fortier, G.; Radu, I.-I. Efficient Synthesis of (−)-trans-Kumausyne via Tandem Intramolecular Alkoxycarbonylation-Lactonization. J. Org. Chem. 1998, 63, 916–917.
  12. Dixon, D.J.; Ley, S.V.; Gracza, T.; Szolcsanyi, P. Total Synthesis of the Polyenoyltetramic acid Mycotoxin Erythroskyrine. J. Chem. Soc. Perkin Trans. 1 1999, 1999, 831–841.
  13. Paddon-Jones, G.C.; Hungerford, N.L.; Haynes, P.; Kitching, W. Efficient Palladium(II)-Mediated Construction of Functionalized Plakortone Cores. Org. Lett. 1999, 1, 1905–1908.
  14. Semmelhack, M.F.; Shanmugam, P. Development of an Approach to the Synthesis of the Plakortones. Tetrahedron Lett. 2000, 41, 3567–3571.
  15. Paddon-Jones, G.C.; McErlean, C.S.P.; Haynes, P.; Moore, C.J.; Konig, W.A.; Kitching, W. Synthesis and Stereochemistry of Some Bicyclic γ-Lactones from Parasitic Wasps (Hymenoptera: Braconidae). Utility of Hydrolytic Kinetic Resolution of Epoxides and Palladium(II)-Catalyzed Hydroxycyclization-Carbonylation-Lactonization of Ene-diols. J. Org. Chem. 2001, 66, 7487–7495.
  16. Haynes, P.Y.; Kitching, W. Total Synthesis and Absolute Stereochemistry of Plakortone D. J. Am. Chem. Soc. 2002, 124, 9718–9719.
  17. Haynes, P.Y.; Kitching, W. Synthesis of the Plakortone Series: Plakortone E. Heterocycles 2004, 62, 173–177.
  18. Babjak, M.; Kapitán, P.; Gracza, T. Synthesis of (+)-Goniothalesdiol and (+)-7-epi-Goniothalesdiol. Tetrahedron 2005, 61, 2471–2479.
  19. Semmelhack, M.F.; Hooley, R.J.; Kraml, C.M. Synthesis of Plakortone B and Analogs. Org. Lett. 2006, 8, 5203–5206.
  20. Boukouvalas, J.; Pouliot, M.; Robichaud, J.; MacNeil, S.; Snieckus, V. Asymmetric Total Synthesis of (−)-Panacene and Correction of Its Relative Configuration. Org. Lett. 2006, 8, 3597–3599.
  21. Kapitán, P.; Gracza, T. Stereocontrolled Oxycarbonylation of 4-Benzyloxyhepta-1,6-diene-3,5-diols Promoted by Chiral Palladium(II) Complexes. Tetrahedron Asymm. 2008, 19, 38–44.
  22. Nesbitt, C.L.; McErlean, C.S.P. An Expedient Synthesis of 2,5-Disubstituted-3-oxygenated Tetrahydrofurans. Tetrahedron Lett. 2009, 50, 6318–6320.
  23. Nesbitt, C.L.; McErlean, C.S.P. Total Synthesis of C19 Lipid Diols Containing a 2,5-Disubstituted-3-Oxygenated Tetrahydrofuran. Org. Biomol. Chem. 2011, 9, 2198–2208.
  24. Haynes, P.Y.; Chow, S.; Rahm, F.; Bernhardt, P.V.; De Voss, J.J.; Kitching, W. Synthesis of the Sponge-Derived Plakortone Series of Bioactive Compounds. J. Org. Chem. 2010, 75, 6489–6501.
  25. Werness, J.B.; Tang, W. Stereoselective Total Synthesis of (−)-Kumausallene. Org. Lett. 2011, 13, 3664–3666.
  26. Markovič, M.; Ďuranová, M.; Koóš, P.; Szolcsányi, P.; Gracza, T. Synthesis of bis-Tetrahydrofuran Subunit of (−)-Neopallavicinin. Tetrahedron 2013, 69, 4185–4189.
  27. Markovič, M.; Koóš, P.; Čarný, T.; Sokoliová, S.; Bohačiková, N.; Moncol’, J.; Gracza, T. Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A. J. Nat. Prod. 2017, 80, 1631–1638.
  28. Markovič, M.; Koóš, P.; Gracza, T. A Short Asymmetric Synthesis of Sauropunols A–D. Synthesis 2017, 49, 2939–2942.
  29. Lopatka, P.; Gavenda, M.; Markovič, M.; Koóš, P.; Gracza, T. Flow Pd(II)-Catalyzed Cyclisation in the Total Synthesis of Jaspine B. Catalysts 2021, 11, 1513.
  30. Kapitán, P.; Gracza, T. Asymmetric Intramolecular Pd(II)-catalyzed Oxycarbonylation of Alkene-1,3-diols. Arkivoc 2008, viii, 8–17.
  31. Doháňošová, J.; Lásikivá, A.; Toffano, M.; Gracza, T.; Vo-Thanh, G. Kinetic Resolution of Pent-4-ene-1,3-diol by Pd(II)-Catalysed Oxycarbonylation in Ionic Liquids. New J. Chem. 2012, 36, 1744–1750.
  32. Babjak, M.; Markovič, K.; Kandríkova, B.; Gracza, T. Homogeneous Cyclocarbonylation of Alkenols with Iron Pentacarbonyl. Synthesis 2014, 46, 809–816.
  33. Markovič, K.; Lopatka, P.; Koóš, P.; Gracza, T. Asymmetric Formal Synthesis of (+)-Pyrenolide D. Synthesis 2014, 46, 817–821.
  34. Lopatka, P.; Markovič, K.; Koóš, P.; Ley, S.V.; Gracza, T. Continuous Pd-Catalyzed Carbonylative Cyclization Using Iron Pentacarbonyl as a CO Source. J. Org. Chem. 2019, 84, 14394–14406.
  35. Babjak, M.; Zálupský, P.; Gracza, T. Regiocontrol in the Palladium(II)-Catalysed Oxycarbonylation of Unsaturated Polyols. Arkivoc 2005, 45, 57.
  36. Tamaru, Y.; Kobayashi, T.; Kawamura, S.; Ochiai, H.; Yoshida, Z. Stereoselective Intramolecular Aminocarbonylation of 3-Hydroxypent-4-enylamides Catalyzed by Palladium. Tetrahedron Lett. 1985, 26, 4479–4482.
  37. Tamaru, Y.; Hojo, M.; Yoshida, Z. Palladium(2+)-Catalyzed Intramolecular Aminocarbonylation of 3-Hydroxy-4-pentenylamines and 4-Hydroxy-5-hexenylamines. J. Org. Chem. 1988, 53, 5731–5741.
  38. Hümmer, W.; Dubois, E.; Gracza, T.; Jäger, V. Halocyclization and Palladium(II)-Catalyzed Amidocarbonylation of Unsaturated Aminopolyols. Synthesis of 1,4-Iminoglycitols as Potential Glycosidase Inhibitors. Synthesis 1997, 1997, 634–642.
  39. Caletková, O.; Ďurišová, N.; Gracza, T. Aminohydroxylation of Divinylcarbinol and its Application to the Synthesis of Bicyclic hydroxypyrrolidine and Aminotetrahydrofuran Building Blocks. Chem. Pap. 2013, 67, 66–75.
  40. Koóš, P.; Špánik, I.; Gracza, T. Asymmetric Intramolecular Pd(II)-Catalysed Amidocarbonylation of Unsaturated Amino Alcohols. Tetrahedron Asymm. 2009, 20, 2720–2723.
  41. Shi, L.; Weng, M.; Li, F. Palladium-Catalyzed Tandem Carbonylative Aza-Wacker-Type Cyclization of Nucleophile Tethered Alkene to Access Fused N-Heterocycles. Chin. J. Chem. 2021, 39, 317–322.
  42. Lee, H.-W.; Kwong, F.-Y. A Decade of Advancements in Pauson-Khand-Type Reactions. Eur. J. Org. Chem. 2010, 2010, 789–811.
  43. Shibata, T. Recent Advances in the Catalytic Pauson-Khand-type Reaction. Adv. Synth. Catal. 2006, 348, 2328–2336.
  44. Blanco-Urgoiti, J.; Añorbe, L.; Pérez-Serrano, L.; Domínguez, G.; Pérez-Castells, J. The Pauson–Khand Reaction, a Powerful Synthetic Tool for the Synthesis of Complex Molecules. Chem. Soc. Rev. 2004, 33, 32–42.
  45. Heravi, M.M.; Mohammadi, L. Application of Pauson-Khand Reaction in the Total Synthesis of Terpenes. RSC Adv. 2021, 11, 38325–38373.
  46. Yang, Z. Navigating the Pauson-Khand Reaction in Total Syntheses of Complex Natural Products. Acc. Chem. Res. 2021, 54, 556–568.
  47. Chen, S.; Jiang, C.; Zheng, N.; Yang, Z.; Shi, L. Evolution of Pauson-Khand Reaction: Strategic Applications in Total Syntheses of Architecturally Complex Natural Products (2016–2020). Catalysts 2020, 10, 1199.
  48. Keese, F.; Guidetti-Grept, R.; Herzog, B. Synthesis of Fenestranes by Pd-Catalyzed Carbonylation-Cyclisation. Tetrahedron Lett. 1992, 33, 1207–1210.
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