Stereoselective total synthesis of (-)-aspinolide B from (R)-2,3-O-isopropylideneglyceraldehyde

Synthesis

Volumn , Issue 23, 2007, Pages 3627-3634

  Krishna, Palakodety Radha ^a   Narsingam, M ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

(R) 2,3 O isopropylideneglyceraldehyde; 1,2 anti selective reduction; Jacobsen hydrolytic kinetic resolution; Sharpless asymmetric epoxidation; Yamaguchi lactonization

Indexed keywords

JACOBSEN HYDROLYTIC KINETIC RESOLUTION; SHARPLESS ASYMMETRIC EPOXIDATION; YAMAGUCHI LACTONIZATION;

EPOXIDATION; KINETICS; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

ALDEHYDES;

2,3 O ISOPROPYLIDENEGLYCERALDEHYDE; ASPINOLIDE B; GLYCERALDEHYDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CHEMICAL STRUCTURE; EPOXIDATION; HYDROLYSIS KINETICS; LACTONIZATION; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 37049010524     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990824     Document Type: Article

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