Literature DB >> 14737566

The intramolecular Baylis-Hillman reaction: easy preparation of versatile substrates, facile reactions, and synthetic applications.

Jung Eun Yeo1, Xiuling Yang, Hee Jin Kim, Sangho Koo.   

Abstract

We have developed a general and highly efficient method for the preparation of diverse [small omega]-formyl-[small alpha],[small beta]-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis-Hillman reactions of these compounds to provide various biologically important polycyclic compounds.

Entities:  

Year:  2003        PMID: 14737566     DOI: 10.1039/b311951c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Cyclization cascades initiated by 1,6-conjugate addition.

Authors:  Joshua L Brooks; Alison J Frontier
Journal:  J Am Chem Soc       Date:  2012-09-28       Impact factor: 15.419

2.  Synthesis of sultam scaffolds via intramolecular oxa-Michael and diastereoselective Baylis-Hillman reactions.

Authors:  Aihua Zhou; Paul R Hanson
Journal:  Org Lett       Date:  2008-06-14       Impact factor: 6.005

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.