Novell synthesis of α-amino carboxamides and their related compounds via α-oxo sulfones starting from 2,2-disulfonyloxiranes

Bulletin of the Chemical Society of Japan

Volumn 77, Issue 10, 2004, Pages 1897-1903

  Matsumoto, Shoji ^a   Ishii, Michiko ^a   Kimura, Kazuto ^a   Ogura, Katsuyuki ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; CONDENSATION; KETONES; OXIDATION; PARAFFINS;

MOLAR AMOUNTS; NUCLEOPHILIC SITES; OXIRANES; SULFONES;

SYNTHESIS (CHEMICAL);

2 (3 METHOXYPHENYL) 3 METHYLSULFONYL 3 (4 TOLYLSULFONYL)OXIRANE; 2 (4 BROMOPHENYL) 3 METHYLSULFONYL 3 (4 TOLYLSULFONYL)OXIRANE; 2 (4 METHOXYCARBONYLPHENYL) 3 METHYLSULFONYL 3 (4 TOLYLSULFONYL)OXIRANE; 2 (4 METHYLSULFONYL) 3 PHENYL 2 (4 TOLYLSULFONYL)OXIRANE; 2 METHYLSULFONYL 2 (4 TOLYLSULFONYL)OXIRANE; 2,5 DIAZACYCLOHEXANONE; 2,6 DIAZACYCLOHEPTANONE; 2,7 DIAZACYCLOOCTANONE; ALKANE DERIVATIVE; AMIDE; CYCLOHEPTANE DERIVATIVE; CYCLOHEXANONE DERIVATIVE; CYCLOOCTANE DERIVATIVE; ETHYLENE OXIDE DERIVATIVE; METHYLTHIOMETHYL 4 TOLYLSULFONE; SULFONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTALLIZATION; OXIDATION; POLYMERIZATION; STEREOISOMERISM; SYNTHESIS;

EID: 8444251074     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.77.1897     Document Type: Article

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77. -1.
78. The mechanism for the formation of the sulfinylmorpholines is uncertain at the present time, but it is likely that these products are derived from morpholine and the sulfinic acids that are formed in the reaction (Scheme 3).
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