First stereoselective total synthesis of panaxjapyne C

被引：5
|
作者：
Thakur, Pallavi [1 ]
Kumaraswamy, B. [1 ]
Reddy, G. Raji [1 ]
Bandichhor, Rakeshwar [2 ]
Mukkanti, K. [3 ]
机构：
[1] Maithili Life Sci Pvt Ltd, IDA, Hyderabad 500076, Andhra Pradesh, India
[2] Dr Reddys Labs Ltd, R&D, IPD, Qutubullapur 500073, Andhra Pradesh, India
[3] JNT Univ, Ctr Environm Sci, Inst Sci & Technol, Hyderabad 500072, Andhra Pradesh, India
来源：
TETRAHEDRON LETTERS | 2012年 / 53卷 / 29期
关键词：
Polyacetylene; Araliaceae; Regioselective opening of epoxide; Cadiot-Chodkiewicz cross coupling; L-ascorbic acid; OPLOPANAX; CHEMISTRY; ALKYNES;
D O I：
10.1016/j.tetlet.2012.04.087
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The first stereoselective total synthesis of polyacetylene panaxjapyne C is described. The key reactions include regioselective opening of the epoxide and Cadiot-Chodkiewicz cross-coupling reactions. L-Ascorbic acid was used as a chiral pool material for the construction of the both terminal acetylenes. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码：3703 / 3705
页数：3
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