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PREPARATION AND RING-OPENING REACTIONS OF A 2,3-ANHYDRIDE DERIVED FROM SUCROSE

DOI: 10.1016/0008-6215(86)80005-2

Source and publish data:

Carbohydrate Research p. 53 - 62 (1986)

Update date:2022-07-29

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Authors:

Gurjar, Mukund K.Gurjar, Mukund K.

Hough, LeslieHough, Leslie

Richardson, Anthony C.Richardson, Anthony C.

Sincharoenkul, Lee V.Sincharoenkul, Lee V.

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Article abstract of DOI:10.1016/0008-6215(86)80005-2

Selective tosylation of 6,1',6'-tri-O-tritylsucrose afforded the 2-O-tosyl derivative and not the 3-O-tosyl derivative as previously claimed.Treatment of the 2-tosylate with base afforded mainly (40percent) the 2,3-manno-epoxide together with the 3,4-altr

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Full text of DOI:10.1016/0008-6215(86)80005-2

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Product name:Acetic acid (2S,3S,4R,5R)-4-acetoxy-2-[(2R,3R,4S,5R,6R)-4,5-diacetoxy-3-(toluene-4-sulfonyloxy)-6-trityloxymethyl-tetrahydro-pyran-2-yloxy]-2,5-bis-trityloxymethyl-tetrahydro-furan-3-yl ester

Cas No:105165-71-7

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