Highly enantioselective Michael addition of α-substituted nitrophosphonates to a vinyl sulfone

Synthesis (Germany)

Volumn 45, Issue 12, 2013, Pages 1654-1658

  Chen, Guo Ying ^a   Lu, Yixin ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

cinchona alkaloid; Michael Addition; nitrophosphonate; thiourea; vinyl sulfone

Indexed keywords

CINCHONA ALKALOID; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE MICHAEL ADDITION; MICHAEL ADDITIONS; MICHAEL REACTIONS; NITROPHOSPHONATE; ORGANOCATALYTIC; VINYL SULFONES;

ALKALOIDS; METABOLITES; NITROGEN COMPOUNDS; THIOUREAS;

ADDITION REACTIONS;

ALPHA SUBSTITUTED NITROPHOSPHONIC ACID DERIVATIVE; CINCHONA ALKALOID; DIETHYL [2 NITRO 1 PHENYL 4 (PHENYLSULFONYL)BUTAN 2 YL]PHOSPHONATE; DIETHYL [2 NITRO 4 (PHENYLSULFONYL)BUTAN 2 YL]PHOSPHONATE; DIETHYL [3 NITRO 1 (PHENYLSULFONYL)DODECAN 3 YL]PHOSPHONATE; DIETHYL [3 NITRO 1 (PHENYLSULFONYL)HEXAN 3 YL]PHOSPHONATE; DIETHYL [3 NITRO 1 (PHENYLSULFONYL)OCTAN 3 YL]PHOSPHONATE; DIETHYL [3 NITRO 1 (PHENYLSULFONYL)PENTAN 3 YL]PHOSPHONATE; DIETHYL [4 METHYL 3 NITRO 1 (PHENYLSULFONYL)PENTAN 3 YL]PHOSPHONATE; PHOSPHONIC ACID DERIVATIVE; PHOSPHORAMIDIC ACID; SULFONE DERIVATIVE; THIOUREA; UNCLASSIFIED DRUG; VINYL SULFONE;

ARTICLE; ASYMMETRIC CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOSELECTIVITY; MICHAEL ADDITION;

EID: 84878808148     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0033-1338434     Document Type: Article

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