Preparation of nitriles by the modification of Mitsunobu-Wilk procedure III carbon elongation of hydroxy esters

Mohammed C. Aesa, Gábor Baán, L. Novák, Csaba Szántay

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

An efficient one-step procedure for the conversion of hydroxy esters into the corresponding nitrile esters using triphenylphosphine (PPh3)-diethyl azodicarboxylate (DEAD) in the presence of acetone cyanohydrin is described.

Original languageEnglish
Pages (from-to)909-914
Number of pages6
JournalSynthetic Communications
Volume26
Issue number5
Publication statusPublished - 1996

Fingerprint

Nitriles
Elongation
Esters
Carbon
triphenylphosphine
acetone cyanohydrin

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Preparation of nitriles by the modification of Mitsunobu-Wilk procedure III carbon elongation of hydroxy esters. / Aesa, Mohammed C.; Baán, Gábor; Novák, L.; Szántay, Csaba.

In: Synthetic Communications, Vol. 26, No. 5, 1996, p. 909-914.

Research output: Contribution to journalArticle

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