Events The 1st International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

10.3390/ecsoc-1-02021

This submission belongs to the session a. General Organic Synthesis of the event The 1st International Electronic Conference on Synthetic Organic Chemistry

Published date

01 Sep, 1997

Citation

J. M. Quintela, A. Díaz, S. Conde, M. Ruiz, V. Ojea, M. C. Fernández, Stereoselective Synthesis of 2-Amino-4-phosphono-4-pentenoic Acid Derivatives (AP4 Analogues), in Proceedings of The 1st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1997, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-1-02021

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Stereoselective Synthesis of 2-Amino-4-phosphono-4-pentenoic Acid Derivatives (AP4 Analogues)

M. C. Fernández ¹

V. Ojea ¹

M. Ruiz ¹

S. Conde ¹

A. Díaz ¹

J. M. Quintela ¹

1. Departamento de Química Fundamental e Industrial. Facultade de Ciencias. Universidade da Coruña Campus A Zapateira s/n, A Coruña 15071. Spain.

Abstract

a-Phoshono esters are widely employed substrates in olefin synthesis via Wadsworth-Emmons reaction.[1] Recently, Collignon and et al have described the organostannyl derivatives as useful intermediates in the synthesis of alkenylphosphonates.[2] In this communication we report our preliminary results on the stereoselective synthesis of amino acids containing alkenylphosphonates by using the a-triorganostannylated bislactim ether

Keywords

n/a

Stereoselective Synthesis of 2-Amino-2-methyl-4-phosphonobutanoic Acid Derivatives (MAP4 Analogues)

A Carbodiimide-Mediated Synthesis of Pyrimidothienopyridazine Derivatives via a Tandem Nucleophilic Addition-Intramolecular Hetero Conjugate Addition Annulation Strategy