✦ LIBER ✦

New synthetic route to carboxylic esters from grignard reagents

✍ Scribed by Masakazu Yamashita; Rikisaku Suemitsu

Publisher: Elsevier Science
Year: 1978
Tongue: French
Weight: 96 KB
Volume: 19
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)94579-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A new general synthetic route to bridged

A new general synthetic route to bridged carboxylic ortho esters

✍ E.J. Corey; Natarajan Raju 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 216 KB

A new general synthetic route to bridged

A new general synthetic route to bridged carboxylic ortho esters

✍ E.J. Corey; Natarajan Raju 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 216 KB

Acylation of the readily available 3-methyl-3-hydroxymethyl oxetane Q leads to the corresponding oxetane esters (3 which rearrange smoothly in the presence of boron trifluoride etherate in methylene chloride at -15" to form ortho esters of the 2,6,7-trioxabicyclo[2.2. aloctane series (2). Protectio

A New Versatile Synthesis of Esters from

A New Versatile Synthesis of Esters from Grignard Reagents and Chloroformates.

✍ Daniela Bottalico; Vito Fiandanese; Giuseppe Marchese; Angela Punzi 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

## 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.

One-Pot Synthesis of Homoallylic Ketones

One-Pot Synthesis of Homoallylic Ketones from the Addition of Vinyl Grignard Reagent to Carboxylic Esters.

✍ Karl A. Hansford; James E. Dettwiler; William D. Lubell 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 124 KB 👁 2 views

A convenient synthetic route to phosphat

A convenient synthetic route to phosphate esters from phosphites

✍ Purnanand; B.S. Batra; B.P. Pant 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 120 KB

Dialkyl arylphosphate esters have been synthesized in improved yields by the reaction of dicyclohexylamine salts of substituted phenols with dialkyl hydrogen phosphite and carbon tetrachloride. The reaction proceeds through the corresponding phosphorochloridates. Dialkyl arylphosphate esters form a

Vinylsilyl Grignard reagents as aryne tr

Vinylsilyl Grignard reagents as aryne traps. A new route to (arylalkenyl)silanes.

✍ Thottumkara K. Vinod; Harold Hart 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 176 KB

A general method for preparing (arylalkenyl)siianes via nucleophilic capture of arynes with vinyltrimethylsilyl Grtgnard reagents is described. We recently developed methodology for forming from one to four new aryl-carbon bonds in a one-pot reaction by treating various polyhalobenzenes with aryll