Literature DB >> 16268526

Construction of the cyclovibsanin core via a biogenetically modeled approach.

David P Tilly1, Craig M Williams, Paul V Bernhardt.   

Abstract

[reaction: see text] Construction of the 15-O-methylcyclovibsanin B core was achieved expediently in eight linear steps utilizing a biogenetically modeled approach.

Entities:  

Mesh：

Substances：

Year:  2005        PMID： 16268526     DOI： 10.1021/ol051897d

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


  5 in total

1.  Towards the Total Synthesis of 3-Hydroxyvibsanin E.

Authors:  Brett D Schwartz; Justin R Denton; Paul V Bernhardt; Huw M L Davies; Craig M Williams
Journal:  Synthesis (Stuttg)       Date:  2009-09-01       Impact factor: 3.157

2.  A mechanistic investigation into the zinc carbenoid-mediated homologation reaction by DFT methods: is a classical donor-acceptor cyclopropane intermediate involved?

Authors:  Wilhelm A Eger; Charles K Zercher; Craig M Williams
Journal:  J Org Chem       Date:  2010-11-05       Impact factor: 4.354

3.  A combined DFT and NMR investigation of the zinc organometallic intermediate proposed in the syn-selective tandem chain extension-aldol reaction of β-keto esters.

Authors:  Karelle S Aiken; Wilhelm A Eger; Craig M Williams; Carley M Spencer; Charles K Zercher
Journal:  J Org Chem       Date:  2012-07-03       Impact factor: 4.354

4.  Total Synthesis of (±)-Vibsanin E.

Authors:  Brett D Schwartz; Justin R Denton; Huw M L Davies; Craig M Williams
Journal:  Aust J Chem       Date:  2009       Impact factor: 1.321

5.  End game strategies towards the total synthesis of vibsanin E, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A.

Authors:  Brett D Schwartz; Craig M Williams; Paul V Bernhardt
Journal:  Beilstein J Org Chem       Date:  2008-10-08       Impact factor: 2.883
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.