(±) 4β-amino-2α,3α-dihydroxy-1β-cyclopentanemethanol hydrochloride. Carbocyclic ribofuranosylamine for the synthesis of carbocyclic nucleosides.

Richard C. Cermak; Robert Vince

doi:10.1016/S0040-4039(01)82898-7

(±) 4β-amino-2α,3α-dihydroxy-1β-cyclopentanemethanol hydrochloride. Carbocyclic ribofuranosylamine for the synthesis of carbocyclic nucleosides.

Richard C. Cermak, Robert Vince

Center for Drug Design

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

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Abstract

Carbocyclic ribofuranosylamine, a key intermediate for the synthesis of carbocyclic ribonucleosides, was synthesized by a facile route from the lactam, 2-azabicyclo[2.2.1]hept5-ene-3-one.

Original language	English (US)
Pages (from-to)	2331-2332
Number of pages	2
Journal	Tetrahedron Letters
Volume	22
Issue number	25
DOIs	https://doi.org/10.1016/S0040-4039(01)82898-7
State	Published - 1981

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title = "(±) 4β-amino-2α,3α-dihydroxy-1β-cyclopentanemethanol hydrochloride. Carbocyclic ribofuranosylamine for the synthesis of carbocyclic nucleosides.",

abstract = "Carbocyclic ribofuranosylamine, a key intermediate for the synthesis of carbocyclic ribonucleosides, was synthesized by a facile route from the lactam, 2-azabicyclo[2.2.1]hept5-ene-3-one.",

author = "Cermak, {Richard C.} and Robert Vince",

year = "1981",

doi = "10.1016/S0040-4039(01)82898-7",

language = "English (US)",

volume = "22",

pages = "2331--2332",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "25",

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TY - JOUR

T1 - (±) 4β-amino-2α,3α-dihydroxy-1β-cyclopentanemethanol hydrochloride. Carbocyclic ribofuranosylamine for the synthesis of carbocyclic nucleosides.

AU - Cermak, Richard C.

AU - Vince, Robert

PY - 1981

Y1 - 1981

N2 - Carbocyclic ribofuranosylamine, a key intermediate for the synthesis of carbocyclic ribonucleosides, was synthesized by a facile route from the lactam, 2-azabicyclo[2.2.1]hept5-ene-3-one.

AB - Carbocyclic ribofuranosylamine, a key intermediate for the synthesis of carbocyclic ribonucleosides, was synthesized by a facile route from the lactam, 2-azabicyclo[2.2.1]hept5-ene-3-one.

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U2 - 10.1016/S0040-4039(01)82898-7

DO - 10.1016/S0040-4039(01)82898-7

M3 - Article

AN - SCOPUS:0011871717

SN - 0040-4039

VL - 22

SP - 2331

EP - 2332

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 25

ER -

(±) 4β-amino-2α,3α-dihydroxy-1β-cyclopentanemethanol hydrochloride. Carbocyclic ribofuranosylamine for the synthesis of carbocyclic nucleosides.

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