𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The structure of 2,2-dialkyl-1,3,2-oxathiastannolanes

✍ Scribed by Paul A. Bates; Michael B. Hursthouse; Alwyn G. Davies; Seán D. Slater


Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
663 KB
Volume
325
Category
Article
ISSN
0022-328X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


ChemInform Abstract: 1,1-Dialkyl-2-acyl-
✍ K. N. Zelenin; L. F. Melnikova; I. P. Bezhan; I. V. Lagoda; B. F. Chakchir 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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

Stereoselective synthesis of dialkyl 3-s
✍ Issa Yavari; Anvar Mirzaei; Loghman Moradi; Nargess Hosseini 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 138 KB

The 1:1 intermediate generated by the addition of quinoline to dialkyl acetylenedicarboxylates is trapped by 1,3-indanedione to yield dialkyl 3-spiroindanedione-1,2,3,3a-tetrahydropyrrolo[1,2-a]quinoline-1,2-dicarboxylates in good yields. The structures of these products were confirmed by NMR and si

Azimine. VI. 1-Alkoxycarbony 1-2,3-dialk
✍ Christian Leuenberger; Lienhard Hoesch; André S. Dreiding 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 German ⚖ 769 KB

**Azimines VI: 1‐Alkoxycarbonyl‐2,3‐dialkyl‐ and ‐2,3‐diarylazimines** Alkoxycarbonyl‐nitrenes **2** – generated in situ by α‐elimination from __N__‐[(4‐nitrophenyl)‐sulfonyloxy]carbamates **4** – were reacted with six aliphatic and aromatic azo compounds to yield 1‐alkoxycarbonyl‐azimines **11** (

Microwave-Induced Stereoselective Conver
✍ Ali Ramazani; Akram Abbasi Motejadded; Ebrahim Ahmadi 📂 Article 📅 2006 🏛 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.