Literature DB >> 15806554

Synthetic examination of incorrectly proposed structures of biomolecules.

Kenji Mori1.   

Abstract

Many incorrect structures of biomolecules have been proposed for natural products. Synthesis of compounds having the proposed structures often enabled us to judge the correctness of the proposals. In some cases, we were able to revise the structures by synthesizing the biomolecules themselves. In other cases, we were able to definitely disprove the proposed structures. Some examples treated in this review include: auxin-a and b; the sex pheromone of Chlamydomonas; sex pheromones of the gypsy moth, the American cockroach, and the pink bollworm moth; Persoons' periplanone-A; orobanchol; naurol A; bifurcarenone; koninginin A; alpha-acoradiene; himachalene-type pheromones of the flea beetle; differolide; blattellastanoside A and B; etc. Copyright 2005 The Japan Chemical Journal Forum and Wiley Periodicals, Inc.

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Year:  2005        PMID: 15806554     DOI: 10.1002/tcr.20030

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  1 in total

1.  Homofarnesals: female sex attractant pheromone components of the southern cowpea weevil, Callosobruchus chinensis.

Authors:  Kenji Shimomura; Satoshi Nojima; Shunsuke Yajima; Kanju Ohsawa
Journal:  J Chem Ecol       Date:  2008-03-20       Impact factor: 2.626

  1 in total

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