Photoinduced electron-transfer α-deoxygenation of aldonolactones. Efficient synthesis of 2-deoxy-d-arabino-hexono-1,4-lactone

Carbohydrate Research

Volumn 341, Issue 11, 2006, Pages 1788-1795

  Bordoni, Andrea ^a   de Lederkremer, Rosa M ^a   Marino, Carla ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

2 Deoxy d arabino 1,4 lactone; 2 Deoxy d lyxono 1,4 lactone; Aldonolactone photodeoxygenation; Deoxy sugars

Indexed keywords

CHARGE TRANSFER; IRRADIATION; PHOTOSENSITIZERS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

2-DEOXY-D-ARABINO-1,4-LACTONE; 2-DEOXY-D-LYXONO-1,4-LACTONE; ALDONOLACTONE PHOTODEOXYGENATION; DEOXY SUGARS;

ELECTRONS;

2 DEOXY 3 O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO ARABINOHEXONO 1,4 LACTONE; 2 DEOXY 3,5,6 TRI O [(3 TRIFLUOROMETHYL)BENZOYL] DEXTRO ARABINOHEXONO 1,4 LACTONE; 2 DEOXY 6 O [(3 TRIFLUOROMETHYL)BENZOYL] DEXTRO ARABINOHEXONO 1,4 LACTONE; 2 DEOXY DEXTRO ARABINOHEXONO 1,4 LACTONE; 2 O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; 2 O BENZOYL DEXTRO GLUCONO 1,4 LACTONE; 2,3 DI O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; 2,3,5,6 TETRA O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; 2,6 DI O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; 3,5 DI O ACETYL 2 DEOXY 6 O [(3 TRIFLUOROMETHYL)BENZOYL] DEXTRO ARABINOHEXONO 1,4 LACTONE; 3,5 DI O ACETYL 2,6 DI O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; 5,6 DI O ISOPROPYLIDINE 2 O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; 5,6 DI O ISOPROPYLIDINE 2,3 DI O [3 (TRIFLUOROMETHYL)BENZOYL] DEXTRO GLUCONO 1,4 LACTONE; ARABINOSE DERIVATIVE; CARBAZOLE DERIVATIVE; CARBOHYDRATE DERIVATIVE; ESTER DERIVATIVE; LACTONE DERIVATIVE; PHOTOSENSITIZING AGENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL PROCEDURES; CHEMICAL REACTION; DEOXYGENATION; ELECTRON TRANSPORT; IRRADIATION; LIGHT; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS;

DEOXY SUGARS; ELECTRON TRANSPORT; GLUCURONATES; LACTONES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; MONOSACCHARIDES; PHOTOCHEMISTRY; SUGAR ACIDS;

EID: 33744986260     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2006.04.012     Document Type: Article

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