Stereoselective synthesis of (-)-bulgecinine hydrochloride and its C-2 epimer from L-ascorbic acid

被引：10

作者：

Chandrasekhar, Srivari ^{[1
]}

Chandrashekar, Gudise

Vijeender, Kandi

Sarma, Ganti Dattatreya

机构：

[1] Indian Inst Chem Technol, Organ Div 1, Hyderabad 500007, Andhra Pradesh, India

[2] Indian Inst Chem Technol, Nucl Magnet Resonance Div, Hyderabad 500007, Andhra Pradesh, India

来源：

TETRAHEDRON-ASYMMETRY | 2006年 / 17卷 / 20期

关键词：

D O I：

10.1016/j.tetasy.2006.10.033

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

An efficient strategy for the stereocontrolled synthesis of (-)-bulgecinine hydrochloride I was accomplished by utilizing a Wittig Horner olefination, stereoselective reduction of the double bond and intramolecular N-alkylation to furnish the target. (c) 2006 Elsevier Ltd. All rights reserved.

引用

页码：2864 / 2869

页数：6

共 56 条

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