𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A novel synthesis of 1,3 Thiazetidine-2-one and 1,3-Oxazine-2-one Derivatives

✍ Scribed by Dr. W. Żankowska-Jasińska; M. Burgiel; A. Danel; A. Sygula


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
350 KB
Volume
330
Category
Article
ISSN
1615-4150

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A Novel Three-Component, One-Pot Synthes
✍ Minoo Dabiri; Akram Sadat Delbari; Ayoob Bazgir 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 19 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.

ChemInform Abstract: Novel 1H-2-Benzopyr
✍ Mahmoud R. Mahmoud; Manal M. El-Shahawi; Samira E. Farahat 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 29 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Properties and reactions of substituted
✍ Schwenkkraus, Peter ;Otto, Hans-Hartwig 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 771 KB

## Abstract β‐Sultam‐3‐acetic acid ester 3 prepared from __rac‐S__‐benzyl‐β‐homocysteine is alkylated with bromoacetates yielding diacetates 9 which are transformed into the phenylthio esters 11. The thiazinanone derivatives 12 are obtained from 11 by rearrangement with lithium bis(trimethylsilyl)a

One pot synthesis of [1,3]-oxazine and [
✍ S. Tumtin; I. T. Phucho; A. Nongpiur; R. Nongrum; J. N. Vishwakarma; B. Myrboh; 📂 Article 📅 2010 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 104 KB

## Abstract magnified image A simple and efficient synthesis of substituted benzo [1,3] oxazine and benzo [1,3] thiazine derivatives under conventional heating, as well as microwave irradiation is reported. The compounds were obtained by the reaction of electron rich phenols, formaldehyde, and aro