A convergent approach toward phoslactomycins and leustroducsins

Tetrahedron

Volumn 66, Issue 33, 2010, Pages 6358-6375

  Druais, Valérie ^a   Hall, Michael J ^a   Corsi, Camilla ^b   Wendeborn, Sebastian V ^b   Meyer, Christophe ^a   Cossy, Janine ^a  

^a CNRS   (France)

^b SYNGENTA CROP PROTECTION AG   (Switzerland)

Author keywords

Leustroducsins; Metathesis reactions; Noyori reduction; Phoslactomycins; Wittig rearrangement

Indexed keywords

ALCOHOL DERIVATIVE; ALPHA BETA UNSATURATED DELTA LACTONE; ANTIBIOTIC AGENT; FOSTRIECIN; GRIGNARD REAGENT; KETONE DERIVATIVE; LACTONE DERIVATIVE; LEUSTRODUCSIN A; LEUSTRODUCSIN B; LEUSTRODUCSIN C; LEUSTRODUCSIN H; NATURAL PRODUCT; PHOSLACTOMYCIN A; PHOSLACTOMYCIN B; PHOSLACTOMYCIN C; PHOSLACTOMYCIN D; PHOSLACTOMYCIN DERIVATIVE; PHOSLACTOMYCIN E; PHOSLACTOMYCIN F; PROTEIN SERINE THREONINE KINASE INHIBITOR; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; GRIGNARD REACTION; PRIORITY JOURNAL; RING CLOSING METATHESIS; STEREOCHEMISTRY; STOICHIOMETRY; WITTIG REARRANGEMENT;

EID: 77955655685     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.05.050     Document Type: Article

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