Stereocontrolled synthesis of vicinal diamines by organocatalytic asymmetric mannich reaction of N -protected aminoacetaldehydes: Formal synthesis of (-)-agelastatin A

Journal of the American Chemical Society

Volumn 134, Issue 17, 2012, Pages 7516-7520

  Kano, Taichi ^a   Sakamoto, Ryu ^a   Akakura, Matsujiro ^b   Maruoka, Keiji ^a  

^a KYOTO UNIVERSITY   (Japan)

^b AICHI UNIVERSITY OF EDUCATION   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,2-DIAMINE; AMINOACETALDEHYDE; CHIRAL SYNTHONS; ENAMINES; FORMAL SYNTHESIS; FUNCTIONALIZED; MANNICH REACTIONS; MOLECULAR CATALYSTS; NATURAL PRODUCTS; OPTICALLY ACTIVE; ORGANOCATALYTIC; STEREOCONTROLLED SYNTHESIS;

ALDEHYDES; AMINO ACIDS; BIOACTIVITY; CATALYSIS; SULFUR COMPOUNDS;

STEREOCHEMISTRY;

ACETALDEHYDE; AGELASTATIN A; AMINOACETALDEHYDE; ANISALDEHYDE; DIAMINE; ENAMINE; PROLINE; SULFONAMIDE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC CATALYSIS; DEPROTECTION REACTION; ENANTIOSELECTIVITY; MANNICH REACTION; STEREOCHEMISTRY;

ACETALDEHYDE; ALKALOIDS; CATALYSIS; DIAMINES; IMINES; MODELS, MOLECULAR; OXAZOLIDINONES; PROLINE; STEREOISOMERISM;

EID: 84860820948     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja301120z     Document Type: Article

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