Phosphinic acid-promoted addition reaction of isocyanides to (Z)-hydroximoyl chlorides: efficient synthesis of α-(hydroxyimino)amides

Author:

Soeta Takahiro12345,Takashita Suguru12345,Sakata Yoko12345,Ukaji Yutaka12345

Affiliation:

1. Division of Material Chemistry

2. Graduate School of Natural Science and Technology

3. Kanazawa University

4. Kanazawa 920-1192

5. Japan

Abstract

The reaction of (Z)-hydroximoyl chlorides with isocyanides promoted by phosphinic acid in the presence of triethylamine proceeds smoothly to afford α-(hydroxyimino)amides in good to high yields.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference38 articles.

1. Oxime Amides as a Novel Zinc Binding Group in Histone Deacetylase Inhibitors: Synthesis, Biological Activity, and Computational Evaluation

2. D. T. W. Chu , in Annual Reports in Medical Chemistry, ed. J. A. Bristol, Academic Press, San Diego, 1998, vol. 33, pp. 141–150

3. Über ein neues Kondensations-Prinzip

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