peloruside-a and 3-hydroxybutanal

peloruside-a has been researched along with 3-hydroxybutanal* in 2 studies

Other Studies

2 other study(ies) available for peloruside-a and 3-hydroxybutanal

Article	Year
Dinuclear zinc-ProPhenol-catalyzed enantioselective α-hydroxyacetate aldol reaction with activated ester equivalents. Organic letters, 2013, Sep-06, Volume: 15, Issue:17 An enantioselective α-hydroxyacetate aldol reaction that employs N-acetyl pyrroles as activated ester equivalents and generates syn 1,2-diols in good yield and diastereoselectivity is reported. This dinuclear zinc-ProPhenol-catalyzed transformation proceeds with high enantioselectivity with a wide variety of substrates including aryl, alyl, and alkenyl aldehydes. The resulting α,β-dihydroxy activated esters are versatile intermediates for the synthesis of a variety of carboxylic acid derivatives including amides, esters, and unsymmetrical ketones. Topics: Alcohols; Aldehydes; Bridged Bicyclo Compounds, Heterocyclic; Catalysis; Combinatorial Chemistry Techniques; Esters; Ketones; Lactones; Molecular Structure; Pyrroles; Stereoisomerism; Zinc	2013
Toward the synthesis of (+)-peloruside A via an intramolecular vinylogous aldol reaction. Organic letters, 2012, Jan-06, Volume: 14, Issue:1 The use of the intramolecular vinylogous aldol reaction for the preparation of an advanced intermediate for the synthesis of peloruside A is described. The reaction was applied to compound 19 and proceeds in high yield and good levels of diastereoselectivity. Application of the Achmatowicz reaction to this intermediate provided the corresponding pyranone, a late stage intermediate well positioned for conversion to the natural product. Topics: Aldehydes; Bridged Bicyclo Compounds, Heterocyclic; Cyclization; Lactones; Molecular Structure; Stereoisomerism; Vinyl Compounds	2012

Article

Year

Dinuclear zinc-ProPhenol-catalyzed enantioselective α-hydroxyacetate aldol reaction with activated ester equivalents.

Organic letters, 2013, Sep-06, Volume: 15, Issue:17

An enantioselective α-hydroxyacetate aldol reaction that employs N-acetyl pyrroles as activated ester equivalents and generates syn 1,2-diols in good yield and diastereoselectivity is reported. This dinuclear zinc-ProPhenol-catalyzed transformation proceeds with high enantioselectivity with a wide variety of substrates including aryl, alyl, and alkenyl aldehydes. The resulting α,β-dihydroxy activated esters are versatile intermediates for the synthesis of a variety of carboxylic acid derivatives including amides, esters, and unsymmetrical ketones.

Topics: Alcohols; Aldehydes; Bridged Bicyclo Compounds, Heterocyclic; Catalysis; Combinatorial Chemistry Techniques; Esters; Ketones; Lactones; Molecular Structure; Pyrroles; Stereoisomerism; Zinc

2013

Toward the synthesis of (+)-peloruside A via an intramolecular vinylogous aldol reaction.

Organic letters, 2012, Jan-06, Volume: 14, Issue:1

The use of the intramolecular vinylogous aldol reaction for the preparation of an advanced intermediate for the synthesis of peloruside A is described. The reaction was applied to compound 19 and proceeds in high yield and good levels of diastereoselectivity. Application of the Achmatowicz reaction to this intermediate provided the corresponding pyranone, a late stage intermediate well positioned for conversion to the natural product.

Topics: Aldehydes; Bridged Bicyclo Compounds, Heterocyclic; Cyclization; Lactones; Molecular Structure; Stereoisomerism; Vinyl Compounds

2012