1984Journal of Carbohydrate ChemistryRequires access

Synthesis and Reactions of Carbohydrate Trifluoro-Methanesulfonates (Carbohydrate Triplates)

Roger W. Binkley, Michael G. Ambrose

Open publisher page 77 citations

Abstract

During the past decade a new leaving group, the trifluoromethanesufonate (triflate), has been used increasingly in displacement reactions in carbohydrate chemistry∗. The importance of this group has become progressively more apparent to the synthetic carbohydrate chemist as the examples of triflate displacement have increased. The number of applications of this reaction now has reached a sufficient magnitude that it seems appropriate to review what has been accomplished.

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What this paper is about

During the past decade a new leaving group, the trifluoromethanesufonate (triflate), has been used increasingly in displacement reactions in carbohydrate chemistry∗. The importance of this group has become progressively more apparent to the synthetic carbohydrate chemist as the examples of triflate displacement have increased. The number of applications of this reaction now has reached a sufficient magnitude that it seems appropriate to review what has been accomplished.

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Available abstract

During the past decade a new leaving group, the trifluoromethanesufonate (triflate), has been used increasingly in displacement reactions in carbohydrate chemistry∗. The importance of this group has become progressively more apparent to the synthetic carbohydrate chemist as the examples of triflate displacement have increased. The number of applications of this reaction now has reached a sufficient magnitude that it seems appropriate to review what has been accomplished.

Key concepts: Chemistry, Carbohydrate chemistry, Carbohydrate, Trifluoromethanesulfonate, Group (periodic table), Organic chemistry, Combinatorial chemistry, Catalysis

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