Title of article :
A stereodivergent approach to carbahexofuranoses: synthesis of carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-allofuranose, carba-β-d-idofuranose, carba-α-d-galactofuranose and carba-β-d-talofuranose
Author/Authors :
Kulkarni، نويسنده , , Mukund G. and Borhade، نويسنده , , Ajit S. and Shaikh، نويسنده , , Yunnus B. and Dhondge، نويسنده , , Attrimuni P. and Birhade، نويسنده , , Deekshaputra R. and Dhatrak، نويسنده , , Nagorao R.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Abstract :
A stereodivergent route, starting from d-glyceraldehyde derivative, employing Wittig olefination–Claisen rearrangement protocol is reported for the synthesis of six novel carbahexofuranoses—carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-allofuranose, carba-β-d-idofuranose, carba-α-d-galactofuranose and carba-β-d-talofuranose in enantiomerically pure form.
Keywords :
Carbasugar , Carbahexofuranose , Claisen rearrangement , Ring closing metathesis
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters
