✦ LIBER ✦

Reaction mechanism of cyclopentadienyliron tricarbonyl cation with cyanate ion

✍ Scribed by Angelici, Robert J.; Charley, Linda M.

Book ID: 126322599
Publisher: American Chemical Society
Year: 1971
Tongue: English
Weight: 409 KB
Volume: 10
Category: Article
ISSN: 0020-1669
DOI: 10.1021/ic50098a043

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reactions of cyclopentadienyliron carbon

Reactions of cyclopentadienyliron carbonyl cations with amines

✍ L. Busetto; R.J. Angelici 📂 Article 📅 1968 🏛 Elsevier Science 🌐 English ⚖ 428 KB

Reactions of some dithiazolium cations w

Reactions of some dithiazolium cations with potassium cyanate

✍ Oliver, James E.; Bierl, Barbara A.; Ruth, John M. 📂 Article 📅 1972 🏛 American Chemical Society 🌐 English ⚖ 406 KB

Photolysis of vinyl halides. Reaction of

Photolysis of vinyl halides. Reaction of photogenerated vinyl cations with cyanate and thiocyanate ions

✍ Kitamura, Tsugio; Kobayashi, Shinjiro; Taniguchi, Hiroshi 📂 Article 📅 1990 🏛 American Chemical Society 🌐 English ⚖ 625 KB

Reactions of the cyclopentadienylrutheni

Reactions of the cyclopentadienylruthenium tricarbonyl cation with nucleophiles

✍ Alan E. Kruse; Robert J. Angelici 📂 Article 📅 1970 🏛 Elsevier Science 🌐 English ⚖ 764 KB

Reaction of tricarbonyl(η6-cycloheptatri

Reaction of tricarbonyl(η6-cycloheptatriene)manganese cation with phosphorus ylides

✍ Si-geun Lee; Young Keun Chung; Tae-Sung Yoon; Whanchul Shin 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 513 KB

Reaction of cationic 1-substituted (η5-4

Reaction of cationic 1-substituted (η5-4-methoxycyclohexadienyl)(tricarbonyl)iron Complexes with anilines: A revised mechanism

✍ Catherine Guillou; Fabrice Bintein; Jean-Philippe Biron; Claude Thal 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 165 KB

Reaction of p-anisidine 13 or p-bromo orthoanisidine 14 with the new bi-deuterated dienyl complex 12 bearing a leaving group on its side chain affords the mono-deuterated 18a, 19a and the non-deuterated lgb and 19b spiro[1,2,3,4-tetrahydroquinoline-4,1'-cyclohexane] derivatives. The formation of the