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Journal articles

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

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.
Keywords : SYNTHESE
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Contributor : Denis Roura Connect in order to contact the contributor
Submitted on : Thursday, March 13, 2014 - 9:22:30 PM
Last modification on : Thursday, December 9, 2021 - 2:26:02 PM

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



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