Theoretical studies of stereoselectivities in the direct anti-Mannich and syn-aldol reactions catalyzed by axially chiral amino sulfonamide

Journal of Molecular Catalysis A: Chemical

Volumn 314, Issue 1-2, 2009, Pages 1-9

  Fu, Aiping ^a   Li, Hongliang ^a   Chu, Tianshu ^a   Zou, Hanxun ^a   Feng, Peng ^a   Yuan, Shuping ^a   Duan, Yunbo ^a  

^a The Growing Base for State Key Laboratory   (China)

Author keywords

Amino sulfonamide; Anti Mannich; Organocatalyst; Syn aldol; Transition structure

Indexed keywords

ALDOL REACTIONS; C-C BONDS; DENSITY FUNCTIONAL THEORY METHODS; DIASTEREOMERIC RATIOS; DIASTEREOSELECTIVITIES; ENAMINE INTERMEDIATES; ENANTIOMERIC EXCESS; ORGANOCATALYSTS; THEORETICAL STUDY; TRANSITION STATE; TRANSITION STRUCTURES;

ALDEHYDES; AMINATION; CHEMICAL BONDS; DENSITY FUNCTIONAL THEORY; STEREOSELECTIVITY; SULFUR COMPOUNDS;

AMINES;

EID: 71749088922     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2009.08.026     Document Type: Article

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