Isosteviol-proline conjugates as highly efficient amphiphilic organocatalysts for asymmetric three-component Mannich reactions in the presence of water

Helvetica Chimica Acta

Volumn 95, Issue 1, 2012, Pages 43-51

  An, Ya Jie ^a,b   Wang, Chuan Chuan ^a   Liu, Zi Ping ^a   Tao, Jing Chao ^a  

^a ZHENGZHOU UNIVERSITY   (China)

^b Henan Commerce Science Institute CoLtd   (China)

Author keywords

Asymmetric synthesis; Catalysis; Isosteviol; Mannich reaction; Multicomponent reactions; Organocatalysts; Proline

Indexed keywords

ASYMMETRIC SYNTHESIS; ISOSTEVIOL; MANNICH REACTION; MULTI-COMPONENT REACTIONS; ORGANOCATALYSTS; PROLINE;

ALDEHYDES; CATALYSIS; SYNTHESIS (CHEMICAL);

AMINO ACIDS;

4 [(16,18 DIOXOBEYERAN 18 YL)OX]PROLINE; 4 [[(16AALPHA) 16 HYDROXY 18 DIOXOBEYERAN 18 YL]OX]PROLINE; ALDEHYDE; AMINO ACID DERIVATIVE; ANILINE DERIVATIVE; CYCLOHEXANONE; O (16,18 DIOXOBEYERAN 18 YL)SERINE; O (16,18 DIOXOBEYERAN 18 YL)THREONINE; O [(16ALPHA) 16 HYDROXY 18 OXOBEYERAN 18 YL]SERINE; O [(16ALPHA) 16 HYDROXY 18 OXOBEYERAN 18 YL]THREONINE; PROLINE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; CONJUGATION; ENANTIOSELECTIVITY; MANNICH REACTION; POLYMERIZATION; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS;

EID: 84862908281     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201100265     Document Type: Article

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