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Volumn 48, Issue 45, 2007, Pages 8037-8039
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A convenient synthesis of 1,2,4-trisubstituted azetidines by reductive cyclization of aza-Michael adducts of chalcones
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Author keywords
Azetidines; Chalcones; Cyclization reactions; Michael addition; Phosphoramidates; Reduction
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Indexed keywords
AZETIDINE DERIVATIVE;
CHALCONE DERIVATIVE;
HETEROCYCLIC COMPOUND;
SODIUM BOROHYDRIDE;
SODIUM DERIVATIVE;
SODIUM HYDRIDE;
UNCLASSIFIED DRUG;
ARTICLE;
CYCLIZATION;
DIASTEREOISOMER;
DRUG SYNTHESIS;
MICHAEL ADDITION;
ORGANIC CHEMISTRY;
QUANTUM YIELD;
REDUCTION;
STEREOCHEMISTRY;
SUBSTITUTION REACTION;
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EID: 35148890241
PISSN: 00404039
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tetlet.2007.09.044 Document Type: Article |
Times cited : (31)
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References (24)
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