Syntheses and odour descriptions of cyclopropanated compounds 3. 1  Analogues of leaf alcohol, its esters and leaf acetal | Zendy

Kiyota Hiromasa | Zendy; Higashi Emi | Zendy; Takai Takafumi | Zendy; Oritani Takayuki | Zendy; Kuwahara Shigefumi | Zendy

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Syntheses and odour descriptions of cyclopropanated compounds 3. 1 Analogues of leaf alcohol, its esters and leaf acetal

Author(s) -

Kiyota Hiromasa,

Higashi Emi,

Takai Takafumi,

Oritani Takayuki,

Kuwahara Shigefumi

Publication year - 2002

Publication title -

flavour and fragrance journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.393

H-Index - 70

eISSN - 1099-1026

pISSN - 0882-5734

DOI - 10.1002/ffj.1092

Subject(s) - chemistry , cyclopropane , cyclopropanation , acetal , double bond , alcohol , ether , alkyl , organic chemistry , aryl , ethanol , stereochemistry , ring (chemistry) , medicinal chemistry , catalysis

Analogues of leaf alcohol and related compounds, bearing a cyclopropane ring in place of the double bond, were synthesized and their odour characteristics were examined. cis ‐(Ethylcyclopropyl)ethanol was prepared using the Simmons–Smith reaction with leaf alcohol. Ethoxyethyl ether and some alkyl and aryl esters were also prepared. Cyclopropanation of the double bond modified their original odour characteristic without losing the key green note. Copyright © 2002 John Wiley & Sons, Ltd.

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