Asymmetric synthesis of jaspine B (pachastrissamine) via an organocatalytic Aldol reaction as key step

Synthesis

Volumn , Issue 14 SPEC. ISS., 2008, Pages 2278-2282

  Enders, Dieter ^a   Terteryan, Violeta ^a   Paleček, Jiří ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

Aldol reaction; Asymmetric synthesis; Organocatalysis; Pachastrissamine (jaspine B); Proline

Indexed keywords

KETONES; STEREOSELECTIVITY;

ALDOL REACTION; ALDOL REACTIONS; ASYMMETRIC SYNTHESIS; DIHYDROXYACETONE; ENANTIOSELECTIVE; ORGANOCATALYSIS; PACHASTRISSAMINE (JASPINE B); PENTADECANAL; PROLINE;

ELECTRON TRANSITIONS;

1 PENTACADECANAL; 2,2 DIMETHYL 1,3 DIOXAN 5 ONE; ACETYLACETONE; DIHYDROXYACETONE; DIOXANE DERIVATIVE; JASPINE B; PROLINE; SPHINGOSINE DERIVATIVE;

ALDOL REACTION; ARTICLE; ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; CHEMICAL STRUCTURE; COST BENEFIT ANALYSIS; CYCLIZATION; ENANTIOSELECTIVITY; STEREOCHEMISTRY;

EID: 48549105569     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067142     Document Type: Article

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