Enantioselective syntheses of pachastrissamine and jaspine A via hydroxylactonization of a chiral epoxy ester

Bioscience, Biotechnology and Biochemistry

Volumn 74, Issue 1, 2010, Pages 152-157

  Urano, Hiroyuki ^a   Enomoto, Masaru ^a   Kuwahara, Shigefumi ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Cytotoxic; Hetrocycle; Jaspine; Pachastrissamine; Phytosphingosine

Indexed keywords

ACIDIC CONDITIONS; ASYMMETRIC EPOXIDATION; CYTOTOXIC; ENANTIOSELECTIVE SYNTHESIS; ENANTIOSELECTIVE TOTAL SYNTHESIS; EPOXIDE RING OPENING; EPOXY ESTERS; FURANOL; HETROCYCLES; HIGH YIELD; OXAZOLIDINES; PACHASTRISSAMINE (JASPINE B); PHYTOSPHINGOSINES; RING FORMATION; UNSATURATED ALDEHYDES; UNSATURATED ESTERS;

ALDEHYDES; ESTERIFICATION; ESTERS; STEREOCHEMISTRY;

SYNTHESIS (CHEMICAL);

DRUG DERIVATIVE; EPOXIDE; ESTER; FUSED HETEROCYCLIC RINGS; JASPINE A; LACTONE; PACHASTRISSAMINE; SPHINGOSINE;

ARTICLE; CHEMISTRY; CYCLIZATION; ENZYME SPECIFICITY; STEREOISOMERISM; SYNTHESIS;

BICYCLO COMPOUNDS, HETEROCYCLIC; CYCLIZATION; EPOXY COMPOUNDS; ESTERS; LACTONES; SPHINGOSINE; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 75649093391     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.90670     Document Type: Article

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