Stereoselectivity and regioselectivity in nucleophilic ring opening in derivatives of 3-phenylisoxazolo[2,3-a]pyrimidine. Unpredicted dimerization and ring transformation. Syntheses of derivatives of pyrimidinylmethylamine, pyrimidinylmethylamino acid amides, and α-amino-2-pyrimidinylacetamides

Journal of Organic Chemistry

Volumn 69, Issue 15, 2004, Pages 4966-4973

  Zvilichovsky, Gury ^a   Gbara Haj Yahia, Isra ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLATION; DIMERIZATION; ONCOLOGY; REACTION KINETICS; SYNTHESIS (CHEMICAL);

REGIOSELECTIVITY; RING OPENINGS; RING TRANSFORMATION; STEREOSELECTIVITY;

NITROGEN COMPOUNDS;

2 ACETYLIMINO 5,7 DIMETHYL 3 PHENYLISOXAZOLO[2,3 A]PYRIMIDINE; 2 OXO 3 PHENYLISOXAZOLO[2,3 A]PYRIMIDINE DERIVATIVE; 2 PYRIMIDINYLACETAMIDE; 5,7 DIMETHYL 2 IMINO 3 PHENYLISOXAZOLO[2,3 A]PYRIMIDINE; ACETAMIDE DERIVATIVE; ACID; ALPHA AMINO 2 PYRIMIDINYLACETAMIDE; AMIDE; AMINE; AMINO ACID; BLEOMYCIN; EPHEDRINE; IMINE; INDOLE DERIVATIVE; ISOXAZOLE DERIVATIVE; METHYLAMINE; OXYGEN; PHENYL GROUP; PYRIMIDINE DERIVATIVE; PYRIMIDINYLMETHYLAMINE; PYRIMIDINYLMETHYLAMINO ACID AMIDE; PYRIMIDOBLAMIC ACID; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; CHEMICAL REACTION; DECARBOXYLATION; DIMERIZATION; DISSOLUTION; HEATING; OPTICAL ROTATION; REACTION ANALYSIS; RING OPENING; RING TRANSFORMATION; STEREOCHEMISTRY; SYNTHESIS;

AMIDES; AMINES; AMINO ACIDS; DIMERIZATION; METHYLAMINES; MOLECULAR STRUCTURE; OXAZOLES; PYRIMIDINES; STEREOISOMERISM;

EID: 3543002240     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0497196     Document Type: Article

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