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- W1969062560 abstract "d and l forms of carba-β-altrose 8, carba-β-mannose 10a, carba-β-idose 12, carba-β-talose 14 derivatives were prepared from (±)-3-cyclohexene-1-carboxylic acid 1. Homochiral diol compounds d-5a and l-5a, which were prepared from 1 via enzyme resolution of (±)-4a, were efficiently transformed to carba-β-altrose derivatives 8 by stereoselective introduction of hydroxyl groups. Oxidation (PCC)/reduction (NaBH4) of 3-OH and/or 4-OH of 8a efficiently gave 10a, 12, and 14 with good stereoselectivity." @default.
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- W1969062560 date "2004-02-01" @default.
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- W1969062560 title "Practical syntheses of enantiopure carbasugars: carba-β-altrose, carba-β-mannose, carba-β-idose, and carba-β-talose derivatives" @default.
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