✦ LIBER ✦

Isomerization of olefins catalysed by Cp2TiCl2/Mg

✍ Scribed by Yanlong Qian; Guisheng Li; Xiaofan Zheng; Yao-Zeng Huang

Publisher: Elsevier Science
Year: 1993
Weight: 252 KB
Volume: 78
Category: Article
ISSN: 0304-5102
DOI: 10.1016/0304-5102(93)87050-i

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Isomerization of terminal alkenes by the

Isomerization of terminal alkenes by the Cp2TiCl2/Mg/BrCH2CH2Br System

✍ S. Achyutha Rao; M. Periasamy 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 431 KB

Selective hydrogenation of olefins catal

Selective hydrogenation of olefins catalyzed by Cp2TiCl2-iPrMgBr

✍ Yanlong Qian; Guisheng Li; Yao-Zeng Huang 📂 Article 📅 1989 🏛 Elsevier Science ⚖ 199 KB

Studies on olefin isomerization catalyze

Studies on olefin isomerization catalyzed by transition metals: Part IV. Isomerization of 1,5-cyclooctadiene catalyzed by (R-Cp)2TiCl2/R'MgX systems

✍ Qian Yanlong; L'́u; Jiaqui; Xu Weihua 📂 Article 📅 1986 🏛 Elsevier Science ⚖ 368 KB

Studies on olefin isomerization catalyze

Studies on olefin isomerization catalyzed by transition metals: part V. highly selective isomerization of 1,5-hexadiene catalyzed by (R-Cp)2TiCl2/R'MgX

✍ Qian Yanlong; Zhuang Junming; Lu Jiaqi; Hunag Qichen; Xu Weihua; Chen Shoushan 📂 Article 📅 1986 🏛 Elsevier Science ⚖ 234 KB

Cp2TiCl2-Catalyzed Hydroalkylation of α-

Cp2TiCl2-Catalyzed Hydroalkylation of α-Olefins with tBuBr-Et3Al.

✍ I. R. Ramazanov; L. I. Djyachenko; A. G. Ibragimov; U. M. Dzhemilev 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

CP2TiCl2-catalyzed hydroalumination of i

CP2TiCl2-catalyzed hydroalumination of internal alkynes: an access to (Z)-olefins

✍ Arnaud Parenty; Jean-Marc Campagne 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 75 KB

The reduction of alkynols with LiAlH 4 in diglyme is a long known process leading to the formation of (E)-alkenols. We have, by serendipity, found that, in the presence of a catalytic amount (10%) of Cp 2 TiCl 2 , the stereoselectivity of the reaction is reversed, leading to the selective formation