THE SYNTHESIS OF TRANS-CARBOVIR VIA THE RAMBERG-BACKLUND REACTION

A  GRUMANN; H  MARLEY; R J K  TAYLOR

THE SYNTHESIS OF TRANS-CARBOVIR VIA THE RAMBERG-BACKLUND REACTION

A GRUMANN, H MARLEY, R J K TAYLOR

Chemistry

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

Abstract

A novel Ramberg-Backlund approach to the synthesis of 1-amino-4-substituted cyclopentenes is described and applied to prepare the trans-isomer of the carbocyclic nucleoside carbovir.

Original language	English
Pages (from-to)	7767-7768
Number of pages	2
Journal	Tetrahedron Letters
Volume	36
Issue number	42
Publication status	Published - 16 Oct 1995

Keywords

NUCLEOSIDES

Cite this

@article{22500c34e29e4a52bb290aff3741a71b,

title = "THE SYNTHESIS OF TRANS-CARBOVIR VIA THE RAMBERG-BACKLUND REACTION",

abstract = "A novel Ramberg-Backlund approach to the synthesis of 1-amino-4-substituted cyclopentenes is described and applied to prepare the trans-isomer of the carbocyclic nucleoside carbovir.",

keywords = "NUCLEOSIDES",

author = "A GRUMANN and H MARLEY and TAYLOR, {R J K}",

year = "1995",

month = oct,

day = "16",

language = "English",

volume = "36",

pages = "7767--7768",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "42",

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T1 - THE SYNTHESIS OF TRANS-CARBOVIR VIA THE RAMBERG-BACKLUND REACTION

AU - GRUMANN, A

AU - MARLEY, H

AU - TAYLOR, R J K

PY - 1995/10/16

Y1 - 1995/10/16

N2 - A novel Ramberg-Backlund approach to the synthesis of 1-amino-4-substituted cyclopentenes is described and applied to prepare the trans-isomer of the carbocyclic nucleoside carbovir.

AB - A novel Ramberg-Backlund approach to the synthesis of 1-amino-4-substituted cyclopentenes is described and applied to prepare the trans-isomer of the carbocyclic nucleoside carbovir.

KW - NUCLEOSIDES

M3 - Article

SN - 0040-4039

VL - 36

SP - 7767

EP - 7768

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 42

ER -