Atta, Ananta Kumar ; Pathak, Tanmaya (2010) A tandem Michael–SN2-mediated general route to six-membered heterocycles and carbocycles European Journal of Organic Chemistry (35). pp. 6810-6819. ISSN 1434-193X
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.20...
Related URL: http://dx.doi.org/10.1002/ejoc.201000941
Abstract
A powerful, flexible, and stereoselective general strategy for the construction of chirally pure six-membered heterocycles and carbocycles by utilizing a tandem Michael–SN2 sequence is described. The strategy avoids the tedious synthesis of separate starting materials prior to cyclization. The expedient and general strategy, which is virtually untapped until now, will enrich the arsenal of synthetic chemists for the preparation of cyclic compounds.
Item Type: | Article |
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Source: | Copyright of this article belongs to John Wiley and Sons, Inc. |
ID Code: | 104008 |
Deposited On: | 17 Mar 2017 11:46 |
Last Modified: | 17 Mar 2017 11:46 |
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