Literature DB >> 12926922

Triquinanes from linear alkylidene carbenes via trimethylenemethane diyls.

Hee-Yoon Lee1, Yeonjoon Kim.   

Abstract

The intramolecular [2+3] cycloaddition reaction of the trimethylenemethane diyl generated from the intramolecular cyclopropanation reaction of alkylidene carbene produced linearly fused triquinanes regio- and stereoselectively. The current tandem cycloaddition reaction was applied to a 14-step total synthesis of hirsutene from methallyl alcohol.

Entities:  

Year:  2003        PMID: 12926922     DOI: 10.1021/ja036263l

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Total synthesis of (±)-leuconolam: intramolecular allylic silane addition to a maleimide carbonyl group.

Authors:  Enver Cagri Izgu; Thomas R Hoye
Journal:  Chem Sci       Date:  2013-02       Impact factor: 9.825

Review 2.  All-carbon [3 + 2] cycloaddition in natural product synthesis.

Authors:  Zhuo Wang; Junyang Liu
Journal:  Beilstein J Org Chem       Date:  2020-12-09       Impact factor: 2.883

  2 in total

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