Das, Indrajit ; Pal, Tarun K. ; Pathak, Tanmaya (2007) Diastereoselective michael initiated ring closure on vinyl sulfone-modified carbohydrates: a stereospecific and general route to α-substituted cyclopropanes. The Journal of Organic Chemistry, 72 (24). pp. 9181-9189. ISSN 0022-3263
Full text not available from this repository.
Official URL: http://pubs.acs.org/doi/abs/10.1021/jo701378d
Related URL: http://dx.doi.org/10.1021/jo701378d
Abstract
Suitably designed vinyl sulfone-modified furanosides act as substrates for Michael initiated ring closure reactions yielding cyclopropanated carbohydrates. The strategy is general in nature and gives access to cyclopropanes with predefined chiralities on three consecutive carbons with varying substitutions at the α-position.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 104123 |
| Deposited On: | 17 Mar 2017 09:35 |
| Last Modified: | 17 Mar 2017 09:35 |
Repository Staff Only: item control page
