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- W1969102421 abstract "In the first such example, NaBH4 in combination with cyanuric chloride (TCT) has been used to obtain 6-hydroxy-4-benzyl ether derivatives from 4,6-benzylidene acetals of carbohydrates. The nature of hydride donor determines the regioselectivity of acetal opening. High regioselectivity, scope for using a broad range of substrates, functional group tolerance, mild reaction conditions, easy handling process, inexpensive reagents and wide application mark the benefits of the newly developed reagent system." @default.
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- W1969102421 date "2013-11-01" @default.
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- W1969102421 title "Cyanuric chloride/sodium borohydride: a new reagent combination for reductive opening of 4,6-benzylidene acetals of carbohydrates to primary alcohols" @default.
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- W1969102421 doi "https://doi.org/10.1016/j.carres.2013.09.003" @default.
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