Literature DB >> 15895980

Synthetic strategies of marine polycyclic ethers via intramolecular allylations: linear and convergent approaches.

Isao Kadota1, Yoshinori Yamamoto.   

Abstract

Strategies for the synthesis of polycyclic ethers based on intramolecular allylations are overviewed. The intramolecular condensation of allylic stannanes and aldehydes is a powerful tool for the synthesis of oxepane derivatives. The reaction is successfully applied to the iterative total synthesis of hemibrevetoxin B (2). Further, the intramolecular allylation of alpha-acetoxy ethers provides an efficient method for the convergent synthesis of polycyclic ethers. The usefulness of the latter strategy is demonstrated in the convergent total synthesis of gambierol (4).

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Year:  2005        PMID: 15895980     DOI: 10.1021/ar040118a

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  4 in total

1.  Total synthesis of brevetoxin A.

Authors:  Michael T Crimmins; J Lucas Zuccarello; J Michael Ellis; Patrick J McDougall; Pamela A Haile; Jonathan D Parrish; Kyle A Emmitte
Journal:  Org Lett       Date:  2009-01-15       Impact factor: 6.005

2.  Enantioselective total synthesis of brevetoxin A: unified strategy for the B, E, G, and J subunits.

Authors:  Michael T Crimmins; J Michael Ellis; Kyle A Emmitte; Pamela A Haile; Patrick J McDougall; Jonathan D Parrish; J Lucas Zuccarello
Journal:  Chemistry       Date:  2009-09-14       Impact factor: 5.236

3.  Enantioselective total synthesis of brevetoxin A: convergent coupling strategy and completion.

Authors:  Michael T Crimmins; J Lucas Zuccarello; Patrick J McDougall; J Michael Ellis
Journal:  Chemistry       Date:  2009-09-14       Impact factor: 5.236

Review 4.  Bioinspired iterative synthesis of polyketides.

Authors:  Kuan Zheng; Changmin Xie; Ran Hong
Journal:  Front Chem       Date:  2015-05-21       Impact factor: 5.221

  4 in total

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