Literature DB >> 21561137

A concise construction of the chlorahololide heptacyclic core.

Yin-Suo Lu1, Xiao-Shui Peng.   

Abstract

A concise and efficient strategy for the construction of the heptacyclic core of the chloranthaceae family has been developed. The key strategy comprises an S(N)2-type intramolecular nucleophilic substitution and a biomimetic endo-Diels-Alder cycloaddition.

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Year:  2011        PMID: 21561137     DOI: 10.1021/ol2009973

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


  2 in total

1.  A unified strategy toward total syntheses of lindenane sesquiterpenoid [4 + 2] dimers.

Authors:  Biao Du; Zhengsong Huang; Xiao Wang; Ting Chen; Guo Shen; Shaomin Fu; Bo Liu
Journal:  Nat Commun       Date:  2019-04-23       Impact factor: 14.919

2.  Total syntheses of shizukaols A and E.

Authors:  Jian-Li Wu; Yin-Suo Lu; Bencan Tang; Xiao-Shui Peng
Journal:  Nat Commun       Date:  2018-10-02       Impact factor: 14.919

  2 in total

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