Enantiomerically pure allylboronic esters as versatile reagents in the enantioselective synthesis of dihydro-α-pyrone-containing natural products

Synthesis (Germany)

Volumn 45, Issue 8, 2013, Pages 1106-1114

  Bartlett, Sean ^a   Böse, Dietrich ^b   Ghori, Daniel ^b   Mechsner, Bastian ^b   Pietruszka, Jörg ^b  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

^b HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

allyl addition; boronic ester; dihydro pyrones; goniothalamin; natural products

Indexed keywords

ALLYL ADDITION; BORONIC ESTERS; DIASTEREOSELECTIVE SYNTHESIS; ENANTIO; ENANTIOPURE; ENANTIOSELECTIVE SYNTHESIS; GONIOTHALAMIN; NATURAL PRODUCTS;

ENANTIOMERS; ESTERIFICATION;

ESTERS;

2 ENE 1,5 DIOL DERIVATIVE; 5,6 DIHYDRO 2H PYRAN 2 ONE DERIVATIVE; ALCOHOL DERIVATIVE; ALLYLBORONIC ESTER DERIVATIVE; CINNAMALDEHYDE; DIHYDRO ALPHA PYRONE DERIVATIVE; ESTER DERIVATIVE; GONIOTHALAMIN; LACTONE; MASSOIA LACTONE; NATURAL PRODUCT; PARASORBIC ACID; PYRONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; DRUG STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; OXIDATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 84876069015     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1318440     Document Type: Article

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