457645-29-3Relevant academic research and scientific papers
Stereodivergent synthesis of 5a-carba-hexopyranoses from carbohydrates via 6-exo-dig radical cyclization: Preparation of 5a-carba-β-D-manno-, α-D-allo-, β-L-talo- and α-L-gulopyranose pentaacetates from D-mannose
Gomez, Ana M.,Moreno, Eduardo,Danelon, Gerardo O.,Valverde, Serafin,Lopez, J. Cristobal
, p. 2961 - 2974 (2007/10/03)
Four carbasugars, 5a-carba-β-D-manno-, α-D-allo-, β-L-talo- and α-L-gulopyranose pentaacetates, have been prepared in a stereodivergent manner from D-mannose. Alkynyl derivatives of 2,3:4,6-di-O-isopropylidene-D-mannopyranose, which are prepared by homolo
Stereodivergent synthesis of carbasugars from D-mannose. Syntheses of 5a-carba-α-D-allose, β-L-talose, and α-L-gulose pentaacetates
Gómez, Ana M.,Moreno, Eduardo,Valverde, Serafín,López, J. Cristóbal
, p. 891 - 894 (2007/10/03)
A stereodivergent entry to 5a-carba-D- and L-pyranoses from a single precursor is described. The approach is based on the selective deoxygenation of polyoxygenated methylcyclohexane intermediates, readily available from radical cyclization of D-mannose de
