Fluorinated Musk Fragrances: The CF2 Group as a Conformational Bias Influencing the Odour of Civetone and (R)-Muscone

被引:27
作者
Callejo, Ricardo [1 ]
Corr, Michael J. [1 ]
Yang, Mingyan [1 ,2 ]
Wang, Mingan [2 ]
Cordes, David B. [1 ]
Slawin, Alexandra M. Z. [1 ]
O'Hagan, David [1 ]
机构
[1] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] China Agr Univ, Dept Appl Chem, Coll Sci, 2 Yuanmingyuan West Rd, Beijing 100193, Peoples R China
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
conformation analysis; macrocycles; musk fragrances; organofluorine chemistry; structure-activity relationships; RING-CLOSING METATHESIS; ENANTIOSELECTIVE CONJUGATE ADDITION; GEM-DIFLUORO COMPOUNDS; MOLECULAR-STRUCTURE; MACROCYCLIC MUSKS; DIFLUOROMETHYLENE GROUP; PRACTICAL SYNTHESIS; EFFICIENT SYNTHESIS; OLEFIN METATHESIS; (R)-(-)-MUSCONE;
D O I
10.1002/chem.201600519
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The difluoromethylene (CF2) group has a strong tendency to adopt corner over edge locations in aliphatic macrocycles. In this study, the CF2 group has been introduced into musk relevant macrocyclic ketones. Nine civetone and five muscone analogues have been prepared by synthesis for structure and odour comparisons. X-ray studies indeed show that the CF2 groups influence ring structure and they give some insight into the preferred ring conformations, triggering a musk odour as determined in a professional perfumery environment. The historical conformational model of Bersuker and co-workers for musk fragrance generally holds, and structures that become distorted from this consensus, by the particular placement of the CF2 groups, lose their musk fragrance and become less pleasant.
引用
收藏
页码:8137 / 8151
页数:15
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