The methoxyallene approach to oxacycles, part 2: Stereoselective synthesis of 2,3-disubstituted oxepanes

Synthesis

Volumn , Issue 3, 2005, Pages 411-414

  Pérez, Manuel ^a   Canoa, Pilar ^a   Gómez, Generosa ^a   Teijeira, Marta ^a   Fall, Yagamare ^a  

^a UNIVERSITY OF VIGO   (Spain)

Author keywords

Methoxyallene; Michael addition; Natural products; Oxepanes; Toxins

Indexed keywords

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION KINETICS; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

2,3-DISUBSTITUTED OXEPANES; PRECURSORS; REDUCING AGENTS; STEREOSELECTIVITY;

ORGANIC COMPOUNDS;

2 (2 HYDROXYETHYL) 3 HYDROXYOXEPANE; ALLENE DERIVATIVE; BICYCLO COMPOUND; IODIDE; METHOXYALLENE; OXEPANE DERIVATIVE; REDUCING AGENT; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CIS ISOMER; DIASTEREOISOMER; MICHAEL ADDITION; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS; TRANS ISOMER;

EID: 14644434439     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-834946     Document Type: Article

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