Synthesis of γ-, δ-, and ε-lactams by asymmetric transfer hydrogenation of N-(tert-butylsulfinyl)iminoesters

Journal of Organic Chemistry

Volumn 78, Issue 8, 2013, Pages 3647-3654

  Guijarro, David ^a   Pablo, Óscar ^a   Yus, Miguel ^a  

^a UNIVERSITY OF ALICANTE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; ALIPHATIC SUBSTITUENTS; ASYMMETRIC TRANSFER HYDROGENATION; CHIRAL AUXILIARIES; HIGH ENANTIOSELECTIVITY; HIGH YIELD; NITROGEN ATOM; SIX-MEMBERED RINGS;

ENANTIOMERS; HYDROGENATION;

AMIDES;

2 PIPERIDONE DERIVATIVE; 5 (4 CHLOROPHENYL)PYRROLIDIN 2 ONE; 5 (4 METHOXYPHENYL)PYRROLIDIN 2 ONE; 6 (2 NAPHTHYL)PIPERIDIN 2 ONE; 6 (2 THIENYL)PIPERIDIN 2 ONE; 7 PHENYLAZEPAN 2 ONE; EPSILON LACTAM DERIVATIVE; ESTER DERIVATIVE; GAMMA LACTAM DERIVATIVE; LACTAM DERIVATIVE; N (TERT BUTYLSULFINYL)IMINOESTER DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC TRANSFER HYDROGENATION; CHEMICAL PROCEDURES; CHEMICAL REACTION; CHIRALITY; CONFORMATIONAL TRANSITION; CYCLIZATION; DESULFINYLATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; HYDROGENATION; REPRODUCIBILITY;

CYCLIZATION; HYDROGENATION; IMINES; LACTAMS; MOLECULAR STRUCTURE; STEREOISOMERISM; SULFHYDRYL COMPOUNDS;

EID: 84876589762     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo400164y     Document Type: Article

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