Literature DB >> 21952851

PtI2-catalyzed tandem 3,3-rearrangement/Nazarov reaction of arylpropargylic esters: synthesis of indanone derivatives.

Huaiji Zheng1, Xingang Xie, Juan Yang, Changgui Zhao, Peng Jing, Bowen Fang, Xuegong She.   

Abstract

An efficient PtI(2)-catalyzed tandem reaction of arylpropargylic esters, involving 3,3-rearrangement and Nazarov reaction, has been developed to produce 3-substituted and 3,3-disubstituted indanone derivatives. This approach provided a pathway to the synthesis of indanone skeletons in natural products.

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Year:  2011        PMID: 21952851     DOI: 10.1039/c1ob06138k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Study on the synthesis of the cyclopenta[f]indole core of raputindole A.

Authors:  Nils Marsch; Mario Kock; Thomas Lindel
Journal:  Beilstein J Org Chem       Date:  2016-02-23       Impact factor: 2.883

  1 in total

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