✦ LIBER ✦

High periselectivity of cyclocoupling reactions of 2-oxyallyl cation with cycloheptatrieneiron tricarbonyl

✍ Scribed by Takashi Ishizu; Kazunobu Harano; Masami Yasuda; Ken Kanematsu

Book ID: 104241583
Publisher: Elsevier Science
Year: 1981
Tongue: French
Weight: 215 KB
Volume: 22
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)90388-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

High periselectivity of 2-oxyallyl catio

High periselectivity of 2-oxyallyl cations: kinetic evidence of the cyclocoupling reaction and its mechanistic aspects

✍ Ishizu, Takashi; Mori, Masato; Kanematsu, Ken 📂 Article 📅 1981 🏛 American Chemical Society 🌐 English ⚖ 757 KB

Observation of periselectivity for the c

Observation of periselectivity for the cyclocoupling reactions of 2-oxyallyl cation with tricarbonyliron complexes of seven-membered-ring unsaturated compounds

✍ Ishizu, Takashi; Harano, Kazunobu; Yasuda, Masami; Kanematsu, Ken 📂 Article 📅 1981 🏛 American Chemical Society 🌐 English ⚖ 683 KB

Regioselective Reactions of 1-Alkylidene

Regioselective Reactions of 1-Alkylidene-2-oxyallyl Cations with Furan: Control of [4 + 3] Cycloaddition, [3 + 2] Cycloaddition, and Electrophilic Substitution

✍ Fujita, Morifumi; Oshima, Makoto; Okuno, Sakuro; Sugimura, Takashi; Okuyama, Tad 📂 Article 📅 2006 🏛 American Chemical Society 🌐 English ⚖ 86 KB

Chemistry of 2-Oxyallyl Cation - Reactio

Chemistry of 2-Oxyallyl Cation - Reaction with Cyclohexa-1,3-diene. Configuration and Conformational Aspects of 2,4-Dimethyl-bicyclo-[3.2.2]-non-6-en-3-one

✍ Acharan S. Narula 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 244 KB

Replacement of SO2Ar in tricarbonyl-5α-(

Replacement of SO2Ar in tricarbonyl-5α-(arylsulphonyl)cyclohexa-1,3-dieneiron complexes: regio- and stereocontrol in reactions of dienyliron cations with some nucleophiles

✍ L.F. Kelly; A.J. Birch 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 201 KB

Regio-and enantiocontrolled bond formation in tricarbonylcyclohexadieneiron complexes is available via the reaction of their derived cations with sodium p-tolylsulphinate followed by nucleophilrdisplacement of S02Ar.