84999-79-1Relevant articles and documents
Catalytic asymmetric synthesis of (S,4E,15Z)-docosa-4,15-dien-1-yn-3-ol, an antitumor marine natural product
Liu, Fei-Peng,Zhong, Jiang-Chun,Zheng, Bing,Li, Shuo-Ning,Gao, Gui,Wang, Zhong-Yu,Li, Min-Yan,Hou, Shi-Cong,Wang, Min,Bian, Qing-Hua
, p. 961 - 965 (2015/09/01)
Abstract An efficient enantioselective total synthesis of an antitumor marine natural product (S,4E,15Z)-docosa-4,15-dien-1-yn-3-ol 1 with 96% ee and 15% overall yield has been achieved; this is the first preparation of 1 via asymmetric catalytic strategy
Studies in pheromone biosynthesis: Preparation of 3H labelled precursors of Drosophila pheromones
Bricard,Kunesch
, p. 2547 - 2558 (2007/10/02)
Two synthetic schemes were designed giving access to tritium labelled potential precursors of Drosophila pheromones. An intermediate in the first scheme allowed the preparation of [3H]-labelled vaccenyl acetate.
Natural Acetylenes. Part 60. Synthesis of C22 and C23 Diacetylenes, Constituents of the Sponge Reniera fulva
Marquez, Maritza Dorta de,Thaller, Viktor
, p. 1268 - 1297 (2007/10/02)
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