𝔖 Bobbio Scriptorium
✦   LIBER   ✦

An efficient general synthesis of ω-olefinic methyl esters

✍ Scribed by Robert M. Scarborough Jr.; Amos B. Smith III

Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
228 KB
Volume
18
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

An efficient general synthesis of 1-(ben
An efficient general synthesis of 1-(benzotriazol-1-yl)alkyl esters
✍ Alan R. Katritzky; Alfredo Pastor; Michael V. Voronkov 📂 Article 📅 1999 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 399 KB 👁 1 views

## Abstract 1‐(Benzotriazol‐1‐yl)alkyl esters 2a‐u were obtained in yields averaging 86% by the direct reaction of various aldehydes with the corresponding __N__‐acylbenzotriazoles in the presence of a catalytic amount of potassium carbonate (10–25 mole %). The procedure was optimized by evaluating

An Efficient Synthesis of Benzo[b][1,8]n
An Efficient Synthesis of Benzo[b][1,8]naphthyridine-3-carboxylic Methyl Esters.
✍ V. Nithyadevi; S. P. Rajendran 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 21 KB

## 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.

An efficient synthesis of benzo[b][1,8]n
An efficient synthesis of benzo[b][1,8]naphthyridine-3-carboxylic methyl esters
✍ V. Nithyadevi; S. P. Rajendran 📂 Article 📅 2006 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 92 KB

## Abstract magnified image Methyl‐3‐(2‐chloroquinolin‐3‐yl)acrylates **5a‐i** on reaction with methyl amine in acetonitrile yielded methyl‐3‐[2‐(methylamino)quinolin‐3‐yl]acrylates **6a‐i**. When, these were followed by the reaction with the Vilsmeier reagent, they afforded methyl benzo[__b__][1,

Stereospecific synthesis of Z olefins be
Stereospecific synthesis of Z olefins bearing an ω-azido group
✍ A. Chhen; M. Vaultier; R. Carrié 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 210 KB

Ylides derived from w-azidoalkyltriphenylphosphonium salts were generated at low temperature. They are stable at -80°C for several hours and react smoothly and stereospecifically with typical aldehydes to form Z-o-azido olefins which are the precursors of w-unsaturated primary and secondary amines.