Uppili, Sundararajan ; Ramamurthy, V. (2001) Enhanced enantio- and diastereoselectivities via confinement: photorearrangement of 2,4-cyclohexadienones included in zeolites Organic Letters, 4 (1). pp. 87-90. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol010245w
Related URL: http://dx.doi.org/10.1021/ol010245w
Abstract
Employing zeolite as the reaction medium, it is possible to change the enantio (from achiral dienones) and diastereo (from chiral dienones) selectivities during the oxa-di-Π-methane rearrangement of 2,4-cyclohexadienones.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 55498 |
| Deposited On: | 18 Aug 2011 11:43 |
| Last Modified: | 18 Aug 2011 11:43 |
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