Literature DB >> 24689198

Simple and short synthesis of trans-(R)-nerolidol, a pheromone component of fruit spotting bug.

C Le Thanh, Kamlesh R Chauhan.   

Abstract

A three-step synthesis of enantiomerically pure (R) and (S)-trans nerolidol from commercially available E,E-fanesol is described. Trans nerolidol is an abundant sesquiterpene in many plant species, almost enantiomerically pure; however, the configuration of chirality is S. There is no natural resource for R-trans nerolidol, which has recently been identified as a pheromone component of the fruit spotting bug Amblypelta lutescens. The simple syntheses reported here will make enantiomerically pure R- and S-trans nerolidol and homologues available for further research and ultimately for use in integrated pest management strategies comprising pheromones.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24689198

Source DB:  PubMed          Journal:  Nat Prod Commun        ISSN: 1555-9475            Impact factor:   0.986


  1 in total

1.  The T296V Mutant of Amorpha-4,11-diene Synthase Is Defective in Allylic Diphosphate Isomerization but Retains the Ability To Cyclize the Intermediate (3R)-Nerolidyl Diphosphate to Amorpha-4,11-diene.

Authors:  Zhenqiu Li; Ruiping Gao; Qinggang Hao; Huifang Zhao; Longbin Cheng; Fang He; Li Liu; Xiuhua Liu; Wayne K W Chou; Huajie Zhu; David E Cane
Journal:  Biochemistry       Date:  2016-11-11       Impact factor: 3.162

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.