madindoline-a and 3-hydroxybutanal

madindoline-a has been researched along with 3-hydroxybutanal* in 1 studies

Other Studies

1 other study(ies) available for madindoline-a and 3-hydroxybutanal

Article	Year
Asymmetric aldol reaction of acetaldehyde and isatin derivatives for the total syntheses of ent-convolutamydine E and CPC-1 and a half fragment of madindoline A and B. Organic letters, 2009, Sep-03, Volume: 11, Issue:17 The asymmetric aldol reaction of isatin derivatives and acetaldehyde has been developed using 4-hydroxydiarylprolinol as a catalyst, affording the aldol products with high enantioselectivity, these products being key intermediates in the synthesis of 3-hydroxyindole alkaloids. Short syntheses of ent-convolutamydine E and CPC-1 and a half fragment of madindoline A and B have been accomplished. Topics: Acetaldehyde; Aldehydes; Alkaloids; Bridged Bicyclo Compounds, Heterocyclic; Catalysis; Indoles; Isatin; Models, Molecular; Molecular Structure; Stereoisomerism; Streptomyces	2009

Article

Year

Asymmetric aldol reaction of acetaldehyde and isatin derivatives for the total syntheses of ent-convolutamydine E and CPC-1 and a half fragment of madindoline A and B.

Organic letters, 2009, Sep-03, Volume: 11, Issue:17

The asymmetric aldol reaction of isatin derivatives and acetaldehyde has been developed using 4-hydroxydiarylprolinol as a catalyst, affording the aldol products with high enantioselectivity, these products being key intermediates in the synthesis of 3-hydroxyindole alkaloids. Short syntheses of ent-convolutamydine E and CPC-1 and a half fragment of madindoline A and B have been accomplished.

Topics: Acetaldehyde; Aldehydes; Alkaloids; Bridged Bicyclo Compounds, Heterocyclic; Catalysis; Indoles; Isatin; Models, Molecular; Molecular Structure; Stereoisomerism; Streptomyces

2009