| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1348545 | Tetrahedron: Asymmetry | 2006 | 6 Pages |
Abstract
An efficient strategy for the stereocontrolled synthesis of (â)-bulgecinine hydrochloride 1 was accomplished by utilizing a Wittig Horner olefination, stereoselective reduction of the double bond and intramolecular N-alkylation to furnish the target.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Srivari Chandrasekhar, Gudise Chandrashekar, Kandi Vijeender, Ganti Dattatreya Sarma,