Literature DB >> 16524301

Development of a concise and diversity-oriented approach for the synthesis of plecomacrolides via the diene-ene RCM.

Kui Lu1, Mengwei Huang, Zheng Xiang, Yongxiang Liu, Jiahua Chen, Zhen Yang.   

Abstract

[reaction: see text] A concise synthesis of the core structures of plecomacrolide with ring sizes varying from 16 to 19 atoms was achieved for the first time by the diene-ene ring-closing olefin metathesis reaction. This approach should allow access to the structurally diverse analogues of plecomacrolide.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16524301     DOI: 10.1021/ol060221v

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Motualevic acids and analogs: synthesis and antimicrobial structure-activity relationships.

Authors:  Pradeep Cheruku; Jessica L Keffer; Cajetan Dogo-Isonagie; Carole A Bewley
Journal:  Bioorg Med Chem Lett       Date:  2010-06-09       Impact factor: 2.823

2.  Control of olefin geometry in macrocyclic ring-closing metathesis using a removable silyl group.

Authors:  Yikai Wang; Miguel Jimenez; Anders S Hansen; Eun-Ang Raiber; Stuart L Schreiber; Damian W Young
Journal:  J Am Chem Soc       Date:  2011-05-27       Impact factor: 15.419

Review 3.  Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries.

Authors:  Christopher Cordier; Daniel Morton; Sarah Murrison; Adam Nelson; Catherine O'Leary-Steele
Journal:  Nat Prod Rep       Date:  2008-04-14       Impact factor: 13.423

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.