Chandrasekhar, Srivari ; Chandrashekar, Gudise ; Vijeender, Kandi ; Sarma, Ganti Dattatreya (2006) Stereoselective synthesis of (−)-bulgecinine hydrochloride and its C-2 epimer from l-ascorbic acid Tetrahedron: Asymmetry, 17 (20). pp. 2864-2869. ISSN 09574166
Full text not available from this repository.
Official URL: http://doi.org/10.1016/j.tetasy.2006.10.033
Related URL: http://dx.doi.org/10.1016/j.tetasy.2006.10.033
Abstract
An efficient strategy for the stereocontrolled synthesis of (−)-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.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to Elsevier Ltd |
ID Code: | 131495 |
Deposited On: | 07 Dec 2022 03:33 |
Last Modified: | 07 Dec 2022 03:33 |
Repository Staff Only: item control page