Stereoselective total synthesis of (-)-synrotolide diacetate from d-ribose

Tetrahedron

Volumn 63, Issue 19, 2007, Pages 3995-3999

  Krishna, Palakodety Radha ^a   Reddy, P Srinivas ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Asymmetric allylation; D Ribose; Diastereoselective Grignard reaction; Ring closing metathesis; Synrotolide diacetate; Wittig olefination

Indexed keywords

2 ACETYLOXY 1 (1,2 DIACETYLOXYPROPYL) 4 (6 OXO 3,6 DIHYDRO 2H 2 PYRANYL) 3 BUTENYL ACETATE; ACETOACETIC ACID DERIVATIVE; PYRONE DERIVATIVE; RIBOSE; SYNTROLIDE; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; GRIGNARD REACTION; OLEFINATION; PRIORITY JOURNAL; RING CLOSING METATHESIS; STEREOCHEMISTRY; WITTIG REACTION;

EID: 34047267475     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.03.011     Document Type: Article

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