Synthesis of heterocycles by formal cycloadditions of isocyanides
- PMID: 25504958
- DOI: 10.1002/asia.201403207
Synthesis of heterocycles by formal cycloadditions of isocyanides
Abstract
Synthetic methodology for the synthesis of heterocycles is of continuous and high interest with applications in materials, catalysis, and medicines. Multicomponent reactions are suitable tools to efficiently generate chemically diverse sets of heterocycles with sufficient structural complexity. Especially isocyanides have proven to be particularly versatile building blocks in these one-pot processes. Due to their electronic structure, isocyanides are able to act sequentially or simultaneously as a nucleophile and an electrophile. Traditionally, isocyanides are therefore frequently used in multicomponent chemistry. In the recent literature, numerous reactions have been reported that involve formal cycloadditions of isocyanides with conjugated heterodienes. This Focus Review aims at mapping this reactivity and at providing insight into the relationship between the various reported reaction partners and the observed reactivity modes.
Keywords: combinatorial chemistry; conjugated heterodienes; isocyanides; molecular orbitals; multicomponent reactions.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Similar articles
-
Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes.Acc Chem Res. 2003 Dec;36(12):899-907. doi: 10.1021/ar020258p. Acc Chem Res. 2003. PMID: 14674781
-
Isocyanide-Based Multicomponent Reactions for the Synthesis of Heterocycles.Molecules. 2015 Dec 23;21(1):E19. doi: 10.3390/molecules21010019. Molecules. 2015. PMID: 26703561 Free PMC article. Review.
-
Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles.Acc Chem Res. 2011 Nov 15;44(11):1156-71. doi: 10.1021/ar2000343. Epub 2011 Jul 29. Acc Chem Res. 2011. PMID: 21800828
-
Recent advances in isocyanide-based multicomponent chemistry.Curr Opin Chem Biol. 2002 Jun;6(3):306-13. doi: 10.1016/s1367-5931(02)00328-9. Curr Opin Chem Biol. 2002. PMID: 12023110 Review.
-
Multicomponent reactions for the synthesis of heterocycles.Chem Asian J. 2010 Nov 2;5(11):2318-35. doi: 10.1002/asia.201000310. Chem Asian J. 2010. PMID: 20922748 Review.
Cited by
-
One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction.Beilstein J Org Chem. 2016 Jul 18;12:1487-92. doi: 10.3762/bjoc.12.145. eCollection 2016. Beilstein J Org Chem. 2016. PMID: 27559401 Free PMC article.
-
Mechanochemical synthesis of small organic molecules.Beilstein J Org Chem. 2017 Sep 11;13:1907-1931. doi: 10.3762/bjoc.13.186. eCollection 2017. Beilstein J Org Chem. 2017. PMID: 29062410 Free PMC article. Review.
-
Access to 1-amino-3,4-dihydroisoquinolines via palladium-catalyzed C-H bond aminoimidoylation reaction from functionalized isocyanides.RSC Adv. 2019 Dec 18;9(72):42072-42076. doi: 10.1039/c9ra09139d. eCollection 2019 Dec 18. RSC Adv. 2019. PMID: 35542878 Free PMC article.
-
A practical and efficient approach to imidazo[1,2-a]pyridine-fused isoquinolines through the post-GBB transformation strategy.Beilstein J Org Chem. 2017 May 4;13:817-824. doi: 10.3762/bjoc.13.82. eCollection 2017. Beilstein J Org Chem. 2017. PMID: 28546839 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources