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« Previous Abstract"Synthesis of the four stereoisomers of 7-acetoxy-15-methylnonacosane, a component of the female sex pheromone of the screwworm fly, Cochliomyia hominivorax"    Next AbstractSignificance of chirality in pheromone science »

Chem Rec


Title:Synthetic examination of incorrectly proposed structures of biomolecules
Author(s):Mori K;
Address:"Glycosphingolipid Synthesis Group, Laboratory for Immune Regulation, RIKEN Research Center for Allergy and Immunology, c/o Seikagaku Corporation, 3-1253 Tateno, Higashiyamato-shi, Tokyo 207-0021, Japan. mori-riken@crocus.ocn.ne.jp"
Journal Title:Chem Rec
Year:2005
Volume:5
Issue:1
Page Number:1 - 16
DOI: 10.1002/tcr.20030
ISSN/ISBN:1527-8999 (Print) 1528-0691 (Linking)
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"
Keywords:Animals Biochemistry/*methods Biological Factors/*chemical synthesis/*chemistry Molecular Conformation Stereoisomerism;
Notes:"MedlineMori, Kenji eng Review 2005/04/05 Chem Rec. 2005; 5(1):1-16. doi: 10.1002/tcr.20030"

 
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