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A novel synthetic route to N‐protected 1‐aminoalkylphosphonates

A novel synthetic route to N‐protected 1‐aminoalkylphosphonates Dialkyl and dithioalkyl N‐protected 1‐aminoalkylphosphonates were synthesized using reactions of benzyl carbamate, aldehydes and chlorophosphites, or dithioalkyl chlorophosphite, respectively. This represents a novel synthetic method for 1‐aminoalkylphosphonates. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 11:417–421, 2000 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

A novel synthetic route to N‐protected 1‐aminoalkylphosphonates

Heteroatom Chemistry , Volume 11 (6) – Jan 1, 2000

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References (35)

Publisher
Wiley
Copyright
Copyright © 2000 John Wiley & Sons, Inc.
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/1098-1071(2000)11:6<417::AID-HC10>3.0.CO;2-8
Publisher site
See Article on Publisher Site

Abstract

Dialkyl and dithioalkyl N‐protected 1‐aminoalkylphosphonates were synthesized using reactions of benzyl carbamate, aldehydes and chlorophosphites, or dithioalkyl chlorophosphite, respectively. This represents a novel synthetic method for 1‐aminoalkylphosphonates. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 11:417–421, 2000

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 2000

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