Stereoselective Michael additions of phosphorylated allyl carbanions - Synthesis of functionalized cyclopentylphosphonates and phosphane oxides

European Journal of Organic Chemistry

Volumn , Issue 7, 2001, Pages 1259-1266

  Ruan, Wen Juan ^a   Hassner, Alfred ^b  

^a NANKAI UNIVERSITY   (China)

^b BAR ILAN UNIVERSITY   (Israel)

Author keywords

Methylenecyclopentanes; Phosphane oxides; Phosphonates; Stereoselectivity; 3+2 Michael induced ring closure

Indexed keywords

ALLYL COMPOUND; CYCLOPENTANE DERIVATIVE; ESTER; KETONE; OXIDE; PHOSPHONIC ACID DERIVATIVE; PHOSPHORUS DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; DIASTEREOISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHOSPHORYLATION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0035069680     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200104)2001:7<1259::AID-EJOC1259>3.0.CO;2-D     Document Type: Article

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