Odor and (bio)diversity: Single enantiomers of chiral fragrant substances

被引：34

作者：

Abate, A ^{[1
]}

Brenna, E ^{[1
]}

Fuganti, C ^{[1
]}

Gatti, FG ^{[1
]}

Serra, S ^{[1
]}

机构：

[1] CNR, Ist Chim Riconoscimento Mol, Politecn, Dipartimento Chim Mat & Ingn Chim, I-20131 Milan, Italy

来源：

CHEMISTRY & BIODIVERSITY | 2004年 / 1卷 / 12期

关键词：

D O I：

10.1002/cbdv.200490145

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Our sense of smell is enantioselective. This review reports interesting examples of single stereoisomers of natural and synthetic odorants, prepared via bioorganic routes, that support this statement. This article is the summary of a talk given at the Flavours & Fragrances 2004 conference in Manchester at the MCC/UMIST, 1214 May, 2004.

引用

页码：1888 / 1898

页数：11

共 27 条

[1] Preparation of the enantiomerically enriched isomers of the odorous cyclic ethers Clarycet®, Florol®, and Rhubafuran® by enzymatic catalysis [J].