✦ LIBER ✦

A Direct Synthesis of α-(Hydroxymethyl) and α-Alkyl-vinyl Alkyl Ketones.

✍ Scribed by Jihene Ben Kraiem; Taicir Ben Ayed; Hassen Amri

Publisher: John Wiley and Sons
Year: 2007
Weight: 23 KB
Volume: 38
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200702063

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

📜 SIMILAR VOLUMES

Eliminative Wacker Oxidation: An Efficie

Eliminative Wacker Oxidation: An Efficient Synthesis of α-Alkyl Vinyl Methyl Ketones.

✍ Mukund G. Kulkarni; Saryu I. Davawala; Aniruddha K. Doke; Dnyaneswar D. Gaikwad; 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 24 KB

Regioselective synthesis of Alkyl-methox

Regioselective synthesis of Alkyl-methoxyoxiranes from α-alkyl-α, α', α'-trichlorocyclanones and methanolic sodium methoxide

✍ L. De Buyck; S. Bauwens; N. Schamp 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 132 KB 👁 1 views

Direct Organocatalytic Asymmetric α-Hydr

Direct Organocatalytic Asymmetric α-Hydroxymethylation of Ketones and Aldehydes.

✍ Jesus Casas; Henrik Sunden; Armando Cordova 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

Asymmetric Synthesis of α-Alkyl-α-phenyl

Asymmetric Synthesis of α-Alkyl-α-phenylglycines.

✍ Seung-Han Lee; Eun-Kyung Lee; Soo-Min Jeun 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Synthesis of α-Alkyl- and α,α-Dialkyl-β-

Synthesis of α-Alkyl- and α,α-Dialkyl-β-phenyltryptamines.

✍ B. B. Semenov; Yu. I. Smushkevich 📂 Article 📅 2002 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: New General Synthes

ChemInform Abstract: New General Synthesis of α-Alkoxyketones via α′-Alkylation, α-Alkylation and α,α′-Dialkylation of α-Alkoxyketimines.

✍ Filip Colpaert; Sven Mangelinckx; Maria Teresa Rocchetti; Norbert De Kimpe 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 52 KB 👁 1 views

## Abstract The α‐methoxyketones are prepared via deprotonation of the starting propylidene amine (I) with LDA, followed by reaction with alkyl halides and hydrolysis of the imino functionality.