4-Dimethylamino-N-Triphenylmethylpyridinium Chloride-Reference-Cited by-同舟云学术

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4-Dimethylamino-N-Triphenylmethylpyridinium Chloride

Published:2003-04-28 Issue: Volume: Page:184-184
ISSN:
Container-title:Organic Syntheses
language:
Short-container-title:

Author:

Bhatia Ashok V.¹,Chaudhary Sunil K.²,Hernandez Oscar³

Affiliation:

1. Abbott Laboratories; Chemical Development Department; D-54Z North Chicago IL 60064

2. University of Victoria; Department of Biology; Victoria Canada BC V8W 2Y2

3. U.S. Environmental Protection Agency; Office of Pollution Prevention and Toxics (7402); 401 M Street S.W. Washington, DC 20460

Publisher

John Wiley & Sons, Inc.

Reference10 articles.

1. Le fluoroborate de tritylpyridinium : un reactif efficace de tritylation

2. Use of polymers as protecting groups in organic synthesis. II. Protection of primary alcohol functional groups

3. An efficient procedure for the solid phase tritylation of nucleosides and nucleotides

4. A facile procedure for -tritylation

5. Synthesis of the Sodium Salts of Methyl α-L-Fucopyranoside 2-, 3-, and 4-Sulfates

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