Sureshkumar, Devarajulu and Koutha, Srinivasamurthy and Ganesh, Venkataraman and Chandrasekaran, Srinivasan (2010) Tetrathiomolybdate Mediated Rearrangement of Aziridinemethanol Tosylates: A Thia-Aza-Payne Rearrangement. In: Journal of Organic Chemistry, 75 (16). pp. 5533-5541.
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Abstract
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as the major product and cyclic disulfides as minor product under mild reaction conditions via an unprecedented thia-aza-Payne-type rearrangement. Interestingly, when the reaction of I was carried out with 2-aziridino-cyclohexanol derivatives it resulted in the formation of thia-bicyclo[3.1.1]heptane or dithia-bicyclo[3.2.1]octane derivatives.
Item Type: | Journal Article |
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Additional Information: | Copyright of this article belongs to American Chemical Society. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 06 Sep 2010 11:05 |
Last Modified: | 19 Sep 2010 06:15 |
URI: | http://eprints.iisc.ernet.in/id/eprint/31977 |
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