✦ LIBER ✦

Nucleophilic addition of carbazoles to vinyl esters

✍ Scribed by Yu. P. Shekhirev; V. P. Lopatinskii; V. M. Sutyagin; S. A. Tuzovskaya

Book ID: 112356105
Publisher: Springer US
Year: 1983
Tongue: English
Weight: 520 KB
Volume: 19
Category: Article
ISSN: 0009-3122
DOI: 10.1007/bf00515355

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Nucleophilic addition of phosphine to vi

Nucleophilic addition of phosphine to vinyl sulfoxides

✍ N. K. Gusarova; S. I. Verkhoturova; T. I. Kazantseva; N. A. Chernysheva; V. L. M 📂 Article 📅 2008 🏛 Springer 🌐 English ⚖ 131 KB

Some nucleophilic additions to allyl vin

Some nucleophilic additions to allyl vinyl sulfone

✍ E. N. Prilezhaeva; É. S. Shapiro 📂 Article 📅 1970 🏛 Springer 🌐 English ⚖ 422 KB

ChemInform Abstract: Nucleophilic Additi

ChemInform Abstract: Nucleophilic Addition of Pyrroles to Vinyl Sulfones.

✍ L. N. Sobenina; L. A. Es'kova; A. I. Mikhaleva; D.-S. D. Toryashinova; A. I. Alb 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Nucleophilic Additions to Vinyl Phosphine Oxides.

✍ Bjoern Bartels; Jonathan Clayden; Concepcion Gonzalez Martin; Adam Nelson; Matth 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Self-Promoted Nucleophilic Addition of H

Self-Promoted Nucleophilic Addition of Hexafluoro-2-propanol to Vinyl Ethers.

✍ Andrea Di Salvo; Marc David; Benoit Crousse; Daniele Bonnet-Delpon 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

Self-Promoted Nucleophilic Addition of H

Self-Promoted Nucleophilic Addition of Hexafluoro-2-propanol to Vinyl Ethers

✍ Andrea Di Salvo; Marc David; Benoît Crousse; Danièle Bonnet-Delpon 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 128 KB 👁 2 views

## Abstract In spite of its low nucleophilicity, hexafluoro‐2‐propanol easily adds to vinyl ethers, without catalyst, to afford a range of hexafluoroisopropyloxy acetals. This addition reaction also occurred in the presence of a competitive, more nucleophilic alcohol. Kinetic studies showed the imp