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Volumn 123, Issue 30, 2001, Pages 7228-7232
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Efficient control of the diastereoselectivity and regioselectivity in the singlet-oxygen ene reaction of chiral oxazolidine-substituted alkenes by a remote urea NH functionality: Comparison with dimethyldioxirane and m-chloroperbenzoic acid epoxidations
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Author keywords
[No Author keywords available]
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Indexed keywords
DIASTEREOSELECTIVITY;
AROMATIC COMPOUNDS;
CONFORMATIONS;
HYDROGEN BONDS;
OLEFINS;
OXYGEN;
UREA;
STEREOCHEMISTRY;
3 CHLOROPERBENZOIC ACID;
ALKENE DERIVATIVE;
DIMETHYLDIOXIRANE;
OXAZOLIDINE DERIVATIVE;
SINGLET OXYGEN;
UREA DERIVATIVE;
ARTICLE;
CHIRALITY;
DIASTEREOISOMER;
EPOXIDATION;
HYDROGEN BOND;
STEREOCHEMISTRY;
STEREOSPECIFICITY;
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EID: 0034835105
PISSN: 00027863
EISSN: None
Source Type: Journal
DOI: 10.1021/ja010463k Document Type: Article |
Times cited : (24)
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References (62)
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