Literature DB >> 19707669

Enantioselective synthesis of Anomala osakana pheromone and Janus integer pheromone: a flexible approach to chiral gamma-butyrolactones.

Li Lin1, Qiangyang Zhao, A-Ni Li, Fengbo Ren, Fanzhi Yang, Rui Wang.   

Abstract

The enantioselective synthesis of Anomala osakana pheromone and Janus integer pheromone has been achieved without using any protecting groups. The synthesis involved using an asymmetric alkynylation to obtain gamma-hydroxy-alpha,beta-acetylenic esters with high ee (84%) and yields ( approximately 80%), followed by selective hydrogenation and lactonization in high overall yields (87% and 89%).

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Year:  2009        PMID: 19707669     DOI: 10.1039/b909418k

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


  3 in total

1.  A strategy toward the synthesis of C13-oxidized cembrenolides.

Authors:  Alec Saitman; Steven D E Sullivan; Emmanuel A Theodorakis
Journal:  Tetrahedron Lett       Date:  2013-03-20       Impact factor: 2.415

2.  (R)-desmolactone, a female-produced sex pheromone component of the cerambycid beetle Desmocerus californicus californicus (subfamily Lepturinae).

Authors:  Ann M Ray; Ian P Swift; J Steven McElfresh; Ronald L Alten; Jocelyn G Millar
Journal:  J Chem Ecol       Date:  2012-02-14       Impact factor: 2.626

3.  A General Asymmetric Synthesis of (R)-Matsutakeol and Flavored Analogs.

Authors:  Jia Liu; Honglian Li; Chao Zheng; Shichao Lu; Xianru Guo; Xinming Yin; Risong Na; Bin Yu; Min Wang
Journal:  Molecules       Date:  2017-02-27       Impact factor: 4.411

  3 in total

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