Recent advances in catalytic enantioselective multicomponent reactions - Nunes, P. S. G.; Vidal, H. D. A.; Corrêa, A. G. (Org. Biomol. Chem., 2020)

Recent advances in asymmetric multicomponent reactions (AMCRs) - Ahmadi, T.; Mohammadi Ziarani, G.; Gholamzadeh, P.; Mollabagher, H. (Tetrahedron Asymmetry, 2017)

Recent developments in asymmetric multicomponent reactions - Graaff, C.; Ruijter, E.; Orru, R. V. A. (Chem. Soc. Rev., 2012)

Three-component radical homo Mannich reaction - Shi, S. (Nat. Commun., 2021)

Selective and synergistic cobalt(III)-catalysed three-component C–H bond addition to dienes and aldehydes - Boerth, J. A.; Maity, S.; Williams, S. K.; Mercado, B. Q.; Ellman, J. A. (Nat. Catal., 2018)

Nickel-catalyzed formation of fluorine-containing ketones via the selective cross-trimerization reaction of tetrafluoroethylene, ethylene, and aldehydes - Ohashi, M.; Shirataki, H.; Kikushima, K.; Ogoshi, S. (J. Am. Chem. Soc., 2015)

An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins - Zhou, C.; Emrich, D. E.; Larock, R. C. (Org. Lett., 2003)

The three-component coupling synthesis of prostaglandins - Suzuki, M.; Yanagisawa, A.; Noyori, R. (J. Am. Chem. Soc., 1988)

Isonitriles. II. Compounds with aldehydes or with ketones and monobasic organic acids - Passerini, M. (Gazz. Chim. Ital., 1921)

The α-addition of immonium ions and anions to isonitriles accompanied by secondary reactions - Ugi, I. (Angew. Chem. Int. Ed., 1962)

The Ugi three‐component reaction; a valuable tool in modern organic synthesis - Tripolitsiotis, N. P.; Thomaidi, M.; Neochoritis, C. G. (Eur. J. Org. Chem., 2020)

Catalytic enantioselective Passerini three-component reaction - Wang, S. -. X.; Wang, M. -. X.; Wang, D. -. X.; Zhu, J. (Angew. Chem. Int. Ed., 2008)

Asymmetric phosphoric acid-catalyzed four-component Ugi reaction - Zhang, J. (Science, 2018)

Chiral induction in [2+2+2] cycloaddition reactions - Pla-Quintana, A.; Roglans, A. (Asian J. Org. Chem., 2018)

Alkenes in [2+2+2] cycloadditions - Domínguez, G.; Pérez-Castells, J. (Chem. Eur. J., 2016)

Recent advances in stereoselective [2+2+2] cycloadditions - Amatore, M.; Aubert, C. (Eur. J. Org. Chem., 2015)

Beyond Reppe: building substituted arenes by [2+2+2] cycloadditions of alkynes - Galan, B. R.; Rovis, T. (Angew. Chem. Int. Ed., 2009)

Mori, N., Ikeda, S. & Odashima, K. Chemo- and regioselective cyclotrimerization of monoynes catalyzed by a nickel(0) and zinc(II) phenoxide system. Chem. Commun. 181–182 (2001).

Ruthenium-catalyzed [2+2+2] cycloaddition of three different alkynes - Ura, Y. (J. Mol. Catal. A, 2005)

Ru(II)-catalyzed chemo- and regioselective cyclotrimerization of three unsymmetrical alkynes through boron temporary tether. one-pot four-component coupling via cyclotrimerization/Suzuki–Miyaura coupling - Yamamoto, Y.; Ishii, J. -. I.; Nishiyama, H.; Itoh, K. (J. Am. Chem. Soc., 2004)

Synthesis of fijiolide A via an atropselective paracyclophane formation - Heinz, C.; Cramer, N. (J. Am. Chem. Soc., 2015)

Selective cyclotrimerization of enones and alkynes by a nickel and aluminum catalytic system - Mori, N.; Ikeda, S. -. I.; Sato, Y. (J. Am. Chem. Soc., 1999)

NbCl3-catalyzed three-component [2+2+2] cycloaddition reaction of terminal alkynes, internal alkynes, and alkenes to 1,3,4,5-tetrasubstituted 1,3-cyclohexadienes - Satoh, Y.; Obora, Y. (Org. Lett., 2011)

Nickel-catalyzed three-component [3+2+2] cocyclization of ethyl cyclopropylideneacetate and alkynes—selective synthesis of multisubstituted cycloheptadienes - Komagawa, S.; Saito, S. (Angew. Chem. Int. Ed., 2006)

Liquid enol ethers and acetates as gaseous alkyne equivalents in Rh-catalyzed chemo- and regioselective formal cross-alkyne cyclotrimerization - Hara, H.; Hirano, M.; Tanaka, K. (Org. Lett., 2008)

Nickel-catalyzed three-component [2+2+2] cycloaddition reaction of arynes, alkenes, and alkynes - Qiu, Z.; Xie, Z. (Angew. Chem. Int. Ed., 2009)

Enantioselective construction of bridged multicyclic skeletons: intermolecular [2+2+2] cycloaddition/intramolecular Diels–Alder reaction cascade - Kobayashi, M.; Suda, T.; Noguchi, K.; Tanaka, K. (Angew. Chem. Int. Ed., 2011)

Rhodium-catalyzed [3+2+2] and [2+2+2] cycloadditions of two alkynes with cyclopropylideneacetamides - Yoshida, T. (Angew. Chem. Int. Ed., 2015)

Rhodium-catalyzed [2+2+2] cycloaddition of alkynes for the synthesis of substituted benzenes: catalysts, reaction scope, and synthetic applications - Shibata, Y.; Tanaka, K. (Synthesis, 2012)

Multi-component cycloaddition approaches in the catalytic asymmetric synthesis of alkaloid targets - Perreault, S.; Rovis, T. (Chem. Soc. Rev., 2009)

Highly chemo-, regio-, and enantioselective rhodium-catalyzed cross-cyclotrimerization of two different alkynes with alkenes - Hara, J.; Ishida, M.; Kobayashi, M.; Noguchi, K.; Tanaka, K. (Angew. Chem. Int. Ed., 2014)

Rhodium-catalyzed linear cross-trimerization of two different alkynes with an alkene and two different alkenes with an alkyne - Kobayashi, M.; Tanaka, K. (Chem. Eur. J., 2012)

Rhodium-catalyzed enantioselective [2+2+2] cycloaddition of diynes with unfunctionalized alkenes - Shibata, T. (Tetrahedron, 2007)

Rhodium-catalyzed asymmetric [2+2+2] cycloaddition of α,ω-diynes with unsymmetrical 1,2-disubstituted alkenes - Aida, Y.; Sugiyama, H.; Uekusa, H.; Shibata, Y.; Tanaka, K. (Org. Lett., 2016)

The absolute structure of oryzoxymycin - Hashimoto, T. (J. Antibiot., 1974)

A total synthesis of gliotoxin - Fukuyama, T.; Kishi, Y. (J. Am. Chem. Soc., 1976)

A short enantioselective pathway for the synthesis of the anti-influenza neuramidase inhibitor oseltamivir from 1,3-butadiene and acrylic acid - Yeung, H. S.; Corey, E. J. (J. Am. Chem. Soc., 2006)

Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity - Kim, C. U. (J. Am. Chem. Soc., 1997)

C3-Thia and C3-carba isosteres of a carbocyclic influenza neuraminidase inhibitor, (3R,4R,5S)-4-acetamido-5-amino-3-propoxyl-1-cyclohexene-1-carboxylic acid - Lew, W.; Williams, M. A.; Mendel, D. B.; Escarpe, P. A.; Kim, C. U. (Bioorg. Med. Chem. Lett., 1997)

Direct activation of PP2A for the treatment of tyrosine kinase inhibitor-resistant lung adenocarcinoma - Tohmé, R. (JCI Insight, 2019)

Brazdova, B., Zhang, N., Samoshin, V. V. & Guo, X. Trans-2-aminocyclohexanol as a pH-sensitive conformational switch in lipid amphiphiles. Chem. Commun. 4774 (2008).

Nickel-catalyzed dearomative trans-1,2-carboamination - Hernandez, L. W.; Klöckner, U.; Pospech, J.; Hauss, L.; Sarlah, D. (J. Am. Chem. Soc., 2018)

Asymmetric synthesis of protected cyclohexenylamines and cyclohexenols by rhodium-catalyzed [2+2+2] cycloaddition - Masutomi, K.; Sugiyama, H.; Uekusa, H.; Shibata, Y.; Tanaka, K. (Angew. Chem. Int. Ed., 2016)

Recent advances in biaryl-type bisphosphine ligands - Shimizu, H.; Nagasaki, I.; Saito, T. (Tetrahedron, 2005)

Kinetic study of reductive elimination from the complexes (diphosphine)Pd(R)(CN) - Marcone, J. E.; Moloy, K. G. (J. Am. Chem. Soc., 1998)

Chemo- and regioselective intermolecular cyclotrimerization of terminal alkynes catalyzed by cationic rhodium(I)/modified BINAP complexes: application to one-step synthesis of paracyclophanes - Tanaka, K.; Toyoda, K.; Wada, A.; Shirasaka, K.; Hirano, M. (Chem. Eur. J., 2005)

Palladium-catalyzed C-H activation of tert-butyl groups: a simple synthesis of 1,2-dihydrocyclobutabenzene derivatives - Dyker, G. (Angew. Chem. Int. Ed., 1994)

Palladacycles as reactive intermediates - Dyker, G. (Chem. Ber., 1997)

Effect of the β-substituent with respect to the azido group on the reactivity of methyl (2E)-3-[5-(azidomethyl)-2,2-diethyl-1,3-dioxolan-4-yl]-2-methylprop-2-enoate - Gimalova, F. A. (Russ. J. Org. Chem., 2013)

Systematic exploration of the mechanism of chemical reactions: the global reaction route mapping (GRRM) strategy using the ADDF and AFIR methods - Maeda, S.; Ohno, K.; Morokuma, K. (Phys. Chem. Chem. Phys., 2013)

Mechanistic studies of transition-metal-catalyzed [2+2+2] cycloaddition reactions - Roglans, A.; Pla-Quintana, A.; Solà, M. (Chem. Rev., 2021)

Structure and coordinate bonding nature of nickel(0) and copper(I) carbon dioxide complexes. An ab initio molecular orbital study - Sakaki, S.; Kitaura, K.; Morokuma, K. (Inorg. Chem., 1982)

Mechanistic origin of chemo- and regioselectivity of nickel-catalyzed [3+2+2] cyclization reaction - Komagawa, S.; Wang, C.; Morokuma, K.; Saito, S.; Uchiyama, M. (J. Am. Chem. Soc., 2013)

Some applications of the transition state method to the calculation of reaction velocities, especially in solution - Evans, M. G.; Polanyi, M. (Trans. Faraday Soc., 1935)