Issue 7, 2000
From the journal:

Chemical Communications

Diastereoselective synthesis of α-substituted-γ-butyrolactones of nucleosidesvia [1,5]-C,H insertion reactions of α-diazomalonates of nucleosidesElectronic supplementary information (ESI) available: NMR data for 2b and 6b. See http://www.rsc.org/suppdata/cc/b0/b000524j/

Jinsoo Lim,a   Dong-Joon Choob  and  Yong Hae Kim*a  

* Corresponding authors

a Department of Chemistry, Korea Advanced Institute of Science and Technology, Taejon, Korea.
E-mail: kimyh@sorak.kaist.ac.kr

b Department of Chemistry, College of Liberal Arts and Sciences, Kyung Hee University, Seoul, Korea

Abstract

Diastereoselective and regioselective [1,5]-C,H insertion reactions of 2′-deoxy-3′-diazomalonate nucleosides afforded τ-butyrolactones of nucleosides as chiral synthons for the preparation of 2′-C-branched nucleosides.

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Supplementary files

Article information

DOI
https://doi.org/10.1039/B000524J
Article type
Communication
Submitted
18 Jan 2000
Accepted
23 Feb 2000
First published
17 Mar 2000

Chem. Commun., 2000, 553-554

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Diastereoselective synthesis of α-substituted-γ-butyrolactones of nucleosides via [1,5]-C,H insertion reactions of α-diazomalonates of nucleosides

J. Lim, D. Choo and Y. H. Kim, Chem. Commun., 2000, 553 DOI: 10.1039/B000524J

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