(4<i>E</i>,8<i>Z</i>)-12-Methyloxacyclotetradeca-4,8-dien-2-one and Its 7a-Homologue: Conformationally Constrained Double-Unsaturated Macrocyclic Musks by Ring-Closing Alkyne Metathesis
作者:Philip Kraft、Carola Berthold
DOI:10.1055/s-2008-1032135
日期:2008.2
The double-unsaturated macrocyclic lactones (4 E,8 Z)-12-methyloxacyclotetradeca-4,8-dien-2-one and its 7a-homologue (4 E,9 Z)-13-methyloxacyclopentadeca-4,9-dien-2-one, designed as new potent musk odorants by molecular modeling, were synthesized by ring-closing alkyne metathesis in the presence of 10 mol% of Schrock’s alkylidyne catalyst, and subsequent Lindlar hydrogenation. Demethylation of citronellol
双不饱和大环内酯 (4 E,8 Z)-12-methyloxacyclopentadeca-4,8-dien-2-one 及其 7a-同系物 (4 E,9 Z)-13-methyloxacyclopentadeca-4,9-dien- 2-one 是通过分子模型设计为新型强效麝香气味剂,通过在 10 mol% 的 Schrock 烷撑催化剂存在下闭环炔烃复分解和随后的 Lindlar 氢化合成。由亚硝酸诱导的香茅醇去甲基化提供了 3-methyloct-6-yn-1-ol 结构单元。炔烃复分解的底物是通过香茅醇与 3 E 配置的非 3-en-7-ynoic 酸和 dec-3-en-8-ynoic 酸的 Steglich 酯化制备的,可通过 β,γ-选择性 Knoevenagel 缩合获得相应的炔烃 hept-5-ynal 和 oct-6-ynal,它们分别通过 2-甲基环己-2-烯酮的环氧化物的