Palladium-catalyzed stereospecific synthesis of 2,6-disubstituted tetrahydropyrans: 1,3-Chirality transfer by an intramolecular oxypalladation reaction

Journal of Organic Chemistry

Volumn 71, Issue 12, 2006, Pages 4530-4537

  Kawai, Nobuyuki ^a   Lagrange, Jean Marie ^a   Ohmi, Masashi ^a   Uenishi, Jun'ichi ^a  

^a KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

2,6-DISUBSTITUTED TETRAHYDROPYRANS; CHIRALITY; OXYPALLADATION; STEREOGENIC CENTER;

ALCOHOLS; CATALYSIS; PALLADIUM; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

ORGANOMETALLICS;

6 METHYLTETRAHYDROPYRAN; 6 SILYLOXY 1 HEPTYNE; ACETONITRILE; ALCOHOL; ALDEHYDE; ALKENE; ALKYNE; ALLYL ALCOHOL; CHLORIDE; NON 3 ENE 2,8 DIOL; PALLADIUM; PALLADIUM COMPLEX; PROTON; SILANE DERIVATIVE; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ALKYNYLATION; ARTICLE; CATALYSIS; CHEMICAL REACTION; CHIRALITY; CONFORMATION; CYCLIZATION; DEPROTECTION REACTION; DIASTEREOISOMER; NUCLEOPHILE; OXYPALLADATION REACTION; PRODUCT RECOVERY; REACTION ANALYSIS; REDUCTION; STEREOSPECIFICITY; SYNTHESIS; TEMPERATURE;

CATALYSIS; CYCLIZATION; PALLADIUM; PYRANS; STEREOISOMERISM;

EID: 33744935763     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060415o     Document Type: Article

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