OPTICALLY PURE 3,4-DISUBSTITUED AZETIDINONES FROM SUGARS

DOI: 10.1016/0040-4020(89)80050-X

Source and publish data:

Tetrahedron p. 227 - 232 (1989)

Update date:2022-09-26

Topics: Enantiomer Optically pure Isomer Chiral molecule Sugars

Authors:

Chmielewski, Marek

Kaluza, Zbigniew

Abramski, Wojciech

Grodner, Jacek

Belzecki, Czeslaw

Sedmera, Petr

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Article abstract of DOI:10.1016/0040-4020(89)80050-X

Glycolic cleavage of the vic-diol grouping present in N-benzyl-2-carboxy-2-deoxypento and hexopyranosylaminolactams (5, 6, and 7) with sodium metaperiodate under standard conditions leads to formation of reactive dialdehydes 13 and 14 which upon standing

Full text of DOI:10.1016/0040-4020(89)80050-X

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Product name:(3S, 4S) N-benzyl-3-hydroxymethyl-4-(1',3'-dihydroxyisopropoxy)-azetidinone-2

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