The 1,3-dipolar cycloaddition reaction of chiral carbohydrate-derived nitrone and olefin: Towards long-chain sugars

Carbohydrate Research

Volumn 381, Issue , 2013, Pages 205-214

  Oukani, Hassan ^a,b   Pellegrini Moïse, Nadia ^a   Jackowski, Olivier ^a   Chrétien, Françoise ^a   Chapleur, Yves ^a  

^a UNIVERSITÉ DE LORRAINE   (France)

^b CNRS   (France)

Author keywords

1,3 Dipolar cycloaddition; Chiral nitrone; Chiral olefin; Long chain sugar

Indexed keywords

CHAINS; OLEFINS; SUGARS;

1 ,3-DIPOLAR CYCLOADDITIONS; 1 ,3-DIPOLARCYCLOADDITION; DIOXOLANE RING; FACIAL SELECTIVITY; MODEL REACTIONS; NITRONES; OLEFINIC BOND; UNSATURATED ESTERS;

CYCLOADDITION;

ALKENE; CARBOHYDRATE; CARBON; ESTER; MANNOSE; NITRONE; THREITOL;

ARTICLE; CYCLOADDITION; PRIORITY JOURNAL; SYNTHESIS;

1,3-DIPOLAR CYCLOADDITION; CHIRAL NITRONE; CHIRAL OLEFIN; LONG-CHAIN SUGAR;

ALKENES; CARBOHYDRATES; CYCLIZATION; ESTERS; MICROWAVES; MOLECULAR CONFORMATION; NITROGEN OXIDES; STEREOISOMERISM;

EID: 84886727707     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2013.06.022     Document Type: Article

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