The first synthesis of a 12-membered macrolide natural product via a RCM protocol: determination of absolute stereochemistry

Tetrahedron Asymmetry

Volumn 19, Issue 9, 2008, Pages 1153-1160

  Krishna, Palakodety Radha ^a   Srinivas, Ravula ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

10 HYDROXY 12 METHYL 1 OXACYCLODODECANE 2,5 DIONE; MACROLIDE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; EPIMER; ESTERIFICATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS; STEREOCHEMISTRY;

EID: 43849086107     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.04.016     Document Type: Article

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