✦ LIBER ✦

ChemInform Abstract: Pyrroles and N-Vinylpyrroles from Ketones and Acetylenes: Recent Strides

✍ Scribed by B. A. Trofimov; A. I. Mikhaleva; E. Yu. Schmidt; L. N. Sobenina

Publisher: John Wiley and Sons
Year: 2010
Weight: 15 KB
Volume: 41
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201029252

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: N-Vinylpyrroles as

ChemInform Abstract: N-Vinylpyrroles as Protected Pyrroles.

✍ B. A. TROFIMOV; S. E. KOROSTOVA; S. G. SHEVCHENKO; A. I. MIKHALEVA; N. L. MATEL' 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB

ChemInform Abstract: Synthesis of N-Viny

ChemInform Abstract: Synthesis of N-Vinylpyrroles from N-(2-Hydroxyethyl)pyrroles.

✍ B. F. Kukharev; V. K. Stankevich; V. A. Kukhareva 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

ChemInform Abstract: Oligosubstituted Py

ChemInform Abstract: Oligosubstituted Pyrroles Directly from Substituted Methyl Isocyanides and Acetylenes.

✍ Alexander V. Lygin; Oleg V. Larionov; Vadim S. Korotkov; Armin de Meijere 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 40 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Phosphorus-Containi

ChemInform Abstract: Phosphorus-Containing Heterocyclic Compounds Derived from N-Vinylpyrroles.

✍ A. A. TOLMACHEV; S. I. DOVGOPOLY; A. N. KOSTYUK; E. S. KOZLOV; A. O. PUSHECHNIKO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

ChemInform Abstract: From Ketones to Pyr

ChemInform Abstract: From Ketones to Pyrroles in Two Steps

✍ B. A. TROFIMOV; A. I. MIKHALEVA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB

ChemInform Abstract: Efficient Preparati

ChemInform Abstract: Efficient Preparation of Polyunsaturated and Functionalized Acetylenic Ketones from Alkynylmanganese Bromides.

✍ Gerard Cahiez; Olivier Gager; Alban Moyeux; Blandine Laboue-Bertrand 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

## Abstract The orgnaometal reagents, generated in situ, are stable at room temperature and react smoothly with a broad spectrum of carboxylic acid chlorides.