A one-pot four-component (ABC2) synthesis of macrocycles
- PMID: 12596208
- DOI: 10.1002/anie.200390216
A one-pot four-component (ABC2) synthesis of macrocycles
Similar articles
-
The oxa-Michael reaction: from recent developments to applications in natural product synthesis.Chem Soc Rev. 2008 Jun;37(6):1218-28. doi: 10.1039/b718357g. Epub 2008 Apr 21. Chem Soc Rev. 2008. PMID: 18497934 Review.
-
Enyne metathesis/Brønsted acid-promoted heterocyclization.J Org Chem. 2009 Mar 6;74(5):2193-6. doi: 10.1021/jo802582k. J Org Chem. 2009. PMID: 19203219
-
Organocatalysis by N-heterocyclic carbenes.Chem Rev. 2007 Dec;107(12):5606-55. doi: 10.1021/cr068372z. Epub 2007 Oct 23. Chem Rev. 2007. PMID: 17956132 Review. No abstract available.
-
Single bifunctional ruthenium catalyst for one-pot cyclization and hydration giving functionalized indoles and benzofurans.Chemistry. 2010 Jul 19;16(27):7992-5. doi: 10.1002/chem.201001075. Chemistry. 2010. PMID: 20544759 No abstract available.
-
The synthesis and conformation of oxygenated trianglimine macrocycles.Org Biomol Chem. 2005 Feb 7;3(3):524-37. doi: 10.1039/b414747m. Epub 2005 Jan 10. Org Biomol Chem. 2005. PMID: 15678193
Cited by
-
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway.Chem Sci. 2015 Oct 1;6(10):5446-5455. doi: 10.1039/c5sc01958c. Epub 2015 Jul 7. Chem Sci. 2015. PMID: 29861887 Free PMC article.
-
Stefano Marcaccini: a pioneer in isocyanide chemistry.Mol Divers. 2024 Feb;28(1):335-418. doi: 10.1007/s11030-023-10641-7. Epub 2023 Apr 12. Mol Divers. 2024. PMID: 37043161 Free PMC article. Review.
-
Multicomponent macrocyclization reactions (MCMRs) employing highly reactive acyl ketene and nitrile oxide intermediates.Org Lett. 2011 Sep 2;13(17):4732-5. doi: 10.1021/ol202024a. Epub 2011 Aug 9. Org Lett. 2011. PMID: 21827181 Free PMC article.
-
Macrocycles rapidly produced by multiple multicomponent reactions including bifunctional building blocks (MiBs).Mol Divers. 2005;9(1-3):159-69. doi: 10.1007/s11030-005-1313-y. Mol Divers. 2005. PMID: 15789563
-
A one-pot multicomponent strategy for stereospecific construction of tricyclic pyrrolo[1,2-a]quinolines.Chem Commun (Camb). 2012 Dec 21;48(98):11966-8. doi: 10.1039/c2cc37066b. Chem Commun (Camb). 2012. PMID: 23128187 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources