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

✍ Scribed by Catherine Guillou; Fabrice Bintein; Jean-Philippe Biron; Claude Thal


Book ID
104261570
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
165 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis


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 these products is not the result of a nucleophilic substitution of the leaving group present on cation 12. The vinylogous dienyl a-complex 7 was proposed as the reaction intermediate.


📜 SIMILAR VOLUMES


Reactivity of cationic 1-substituted dic
✍ Nicolas Millot; Catherine Guillou; Claude Thal 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 174 KB

## Nucleophilic addition of malonate anion to cationic l-substituted (r$-4-methoxycyclohexadienyl)Fe(C0)2PPh3 comp!exes 6e-g proceeds predominantIy at the more substituted cyclohexadienyl terminus to afford l,l-disubstituted (q 4-4-methoxy-2.4cyclohexadiene)Fe(CO)2PPh3 complexes 7e-g in good yield