Issue 1, 2001
From the journal:

Chemical Communications

Synthesis of hydrolytically stable porphyrinC- and S-glycoconjugates in high yieldsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b0/b008489l/

Paolo Pasetto,a   Xin Chen,a   Charles Michael Drain*a  and  Richard W. Franck*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, Hunter College and Graduate Center of The City University of New York, 695 Park Avenue, New York, NY 10021, USA.
E-mail: cdrain@shiva.hunter.cuny.edu; rfranck@shiva.hunter.cuny.edu;
Fax: Fax: (212)772-5332
Tel: Phone: (212)650-3791;

Abstract

Two C-glucosyl porphyrins are prepared using Ramberg–Backlund and Lindsey methods for the key conversions, and thiosugars are shown to react with perfluorophenylporphyrins.

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Article information

DOI
https://doi.org/10.1039/B008489L
Article type
Communication
Submitted
18 Oct 2000
Accepted
14 Nov 2000
First published
14 Dec 2000

Chem. Commun., 2001, 81-82

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Synthesis of hydrolytically stable porphyrin C- and S-glycoconjugates in high yields

P. Pasetto, X. Chen, C. M. Drain and R. W. Franck, Chem. Commun., 2001, 81 DOI: 10.1039/B008489L

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