Facile Baylis-Hillman reaction of substituted 3-isoxazolecarbaldehydes: The impact of proximal heteroatom within a heterocycle on the acceleration of reaction
IR@CDRI: CSIR-Central Drug Research Institute, Lucknow
View Archive Info| Field | Value | |
| Creator |
Roy, Amrendra K
Batra, Sanjay |
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| Date |
2007-11-15T07:31:13Z
2007-11-15T07:31:13Z 2003 |
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| Identifier |
Synthesis(2003), 2325-2330
http://hdl.handle.net/123456789/26 |
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| Description |
The fast and facile Baylis-Hillman reaction in substi-tuted 3-isoxazolecarbaldehydes confirms the impact of the proxi-mal heteroatom within a heterocycle towards enhanced reactivity of the formyl group for this reaction
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| Format |
110654 bytes
application/pdf |
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| Language |
en
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| Relation |
CDRI Communication No. 6430
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| Subject |
Baylis-Hillman reaction
3-isoxazolecarbaldehyde DABCO DMAP |
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| Title |
Facile Baylis-Hillman reaction of substituted 3-isoxazolecarbaldehydes: The impact of proximal heteroatom within a heterocycle on the acceleration of reaction
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| Type |
Article
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