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Journal Articles Tetrahedron Letters Year : 2001

A short and efficient synthesis of (+)-calystegine B2

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Abstract

A short synthesis of (+)-calystegine B2 from (D)-glucose has been achieved, which involves as the key step a triple domino zinc-mediated reductive ring-opening, imine formation and allylation reaction of 6-iodoglucopyranose. © 2001 Elsevier Science Ltd.

Dates and versions

hal-00954870 , version 1 (13-03-2014)

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F.-D. Boyer, Issam Hanna. A short and efficient synthesis of (+)-calystegine B2. Tetrahedron Letters, 2001, 42 (7), pp.1275-1277. ⟨10.1016/S0040-4039(00)02262-0⟩. ⟨hal-00954870⟩
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