Basavaiah, Deevi ; Aravindu, Kunche (2007) The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: a facile synthesis of functionalized tri-/ tetracyclic frameworks containing azocine moiety Organic Letters, 9 (13). pp. 2453-2456. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol070380u
Related URL: http://dx.doi.org/10.1021/ol070380u
Abstract
The Baylis-Hillman acetates have been conveniently transformed into tri-/ tetracyclic heterocyclic frameworks containing an important azocine moiety via one-pot multistep protocol involving alkylation, reduction, and cyclization sequence.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 3891 |
| Deposited On: | 18 Oct 2010 09:30 |
| Last Modified: | 17 Jan 2011 04:27 |
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