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Synthèses et relations entre constitution chimique et odeur dans la série des terpényl‐3‐cyclohexanols
Author(s) -
Demole Edouard,
Stoll M.
Publication year - 1964
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19640470713
Subject(s) - chemistry , sandalwood , cyclohexanol , epimer , 2 norbornyl cation , stereochemistry , medicinal chemistry , organic chemistry , catalysis , traditional medicine , medicine
The three 3‐(2, 2, exo ‐3‐trimethyl‐ exo ‐5‐norbornyl)‐ (Ia), 3‐( endo ‐2‐bornyl)‐ (Ib), and 3‐(1, 3, 3‐trimethyl‐ exo ‐6‐norbornyl)‐cyclohexanols (Ic) have been synthesized, and the relationship between their structure and their odour studied. Only the axial epimer of Ia has been found to possess a very strong and typical sandalwood odour.