Chandrasekhara, Srivari ; Chandrashekar, Gudise ; Vijeendera, Kandi ; Dattatreya Sarma, Ganti (2006) Stereoselective synthesis of (−)-bulgecinine hydrochloride and its C-2 epimer from L-ascorbic acid Tetrahedron: Asymmetry, 17 (20). pp. 2864-2869. ISSN 0957-4166
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
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 |
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Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 62380 |
Deposited On: | 22 Sep 2011 03:30 |
Last Modified: | 22 Sep 2011 03:30 |
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