The preparation and reactions of protected glyphosate imidate, thioimidate, and thiono esters from N-[diphenoxyphosphinylmethyl]glycinonitrile: Comparative reactivities of activated carboxylate versus phosphonate esters-Reference-Cited by-同舟云学术

The preparation and reactions of protected glyphosate imidate, thioimidate, and thiono esters from N-[diphenoxyphosphinylmethyl]glycinonitrile: Comparative reactivities of activated carboxylate versus phosphonate esters

Published:1992-06 Issue:3 Volume:3 Page:279-291
ISSN:1042-7163
Container-title:Heteroatom Chemistry
language:en
Short-container-title:Heteroat. Chem.

Author:

Dutra Gerard A.,Finkes Michael J.,Sikorski James A.

Publisher

Wiley

Subject

General Chemistry

Reference39 articles.

1. Discovery, Development and Chemistry of Glyphosate, in & (eds): The Herbicide Glyphosate, Butterworth, Boston, MA, pp. 1-17 (1985).

2. U.S. Patent 4,450,531 (1983).

3. Glyphosate and Related Chemistry, in (ed): Advances in Pesticide Science, Part 2, Pergamon Press, New York, pp 139-147 (1979).

4. U.S. Patent 3,799,758 (1974).

5. U.S. Patent 3,868,407 (1975).

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1. ChemInform Abstract: The Preparation and Reactions of Protected Glyphosate Imidate, Thioimidate, and Thiono Esters from N-(Diphenoxyphosphinylmethyl) glycinonitrile: Comparative Reactivities of Activated Carboxylate versus Phosphonate Esters.;ChemInform;2010-08-20

2. The chemistry of the triazolopyridines: an update;Advances in Heterocyclic Chemistry;2002

3. Chapter 2 The heterocyclic chemistry associated with the herbicide glyphosate;Progress in Heterocyclic Chemistry;1997

4. Volume 8 References;Comprehensive Heterocyclic Chemistry II;1996

5. Bicyclic 5-6 Systems with One Ring Junction Nitrogen Atom: Two Extra Heteroatoms 2:0;Comprehensive Heterocyclic Chemistry II;1996