Stereoselective synthesis of 3-β-D-ribofuranosylpyrazole from 2,3-O-isopropylidene-D-ribose; a new route to pyrazole C-nucleosides

Anthony D. Rycroft; Gurdial Singh; Richard H. Wightman

Stereoselective synthesis of 3-β-D-ribofuranosylpyrazole from 2,3-O-isopropylidene-D-ribose; a new route to pyrazole C-nucleosides

Anthony D. Rycroft
, Gurdial Singh
, Richard H. Wightman

School of Engineering & Physical Sciences

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

Abstract

2,3-O-Isopropylidene-D-ribose has been converted stereoselectively into 3(5)-(ß-D-ribofuranosyl)pyrazole 11, a precursor for the C-nucleoside antibiotics pyrazofurin and formycin.

Original language	English
Pages (from-to)	2667-2668
Number of pages	2
Journal	Journal of the Chemical Society, Perkin Transactions 1
Issue number	21
Publication status	Published - 1995

Cite this

@article{b3134a0b004c4997b67924060255ff7c,

title = "Stereoselective synthesis of 3-β-D-ribofuranosylpyrazole from 2,3-O-isopropylidene-D-ribose; a new route to pyrazole C-nucleosides",

abstract = "2,3-O-Isopropylidene-D-ribose has been converted stereoselectively into 3(5)-({\ss}-D-ribofuranosyl)pyrazole 11, a precursor for the C-nucleoside antibiotics pyrazofurin and formycin.",

author = "Rycroft, \{Anthony D.\} and Gurdial Singh and Wightman, \{Richard H.\}",

year = "1995",

language = "English",

pages = "2667--2668",

journal = "Journal of the Chemical Society, Perkin Transactions 1",

issn = "1472-7781",

publisher = "Chemical Society",

number = "21",

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TY - JOUR

T1 - Stereoselective synthesis of 3-β-D-ribofuranosylpyrazole from 2,3-O-isopropylidene-D-ribose; a new route to pyrazole C-nucleosides

AU - Rycroft, Anthony D.

AU - Singh, Gurdial

AU - Wightman, Richard H.

PY - 1995

Y1 - 1995

N2 - 2,3-O-Isopropylidene-D-ribose has been converted stereoselectively into 3(5)-(ß-D-ribofuranosyl)pyrazole 11, a precursor for the C-nucleoside antibiotics pyrazofurin and formycin.

AB - 2,3-O-Isopropylidene-D-ribose has been converted stereoselectively into 3(5)-(ß-D-ribofuranosyl)pyrazole 11, a precursor for the C-nucleoside antibiotics pyrazofurin and formycin.

UR - https://www.scopus.com/pages/publications/37049085960

M3 - Article

SN - 1472-7781

SP - 2667

EP - 2668

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

IS - 21

ER -

Stereoselective synthesis of 3-β-D-ribofuranosylpyrazole from 2,3-O-isopropylidene-D-ribose; a new route to pyrazole C-nucleosides

Abstract

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