Regioselectivity of alkylation of the naphthalene fragment in the opening of a small ring in 3-ferrocenyl-3-(1-naphthyl)cyclopropene, Z-2-bromo-1-ferrocenyl-1-(1-naphthyl)cyclopropane, and 1-ferrocenyl-1-(1-naphthyl)cyclopropane
✍ Scribed by Elena I. Klimova; Marcos Martı́nez Garcı́a; Tatiana Klimova; Cecilio Alvarez Toledano; Alfredo Ruben Toscano; Rafael Moreno Esparza; Lena Ruı́z Ramı́rez
- Book ID
- 108354596
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 317 KB
- Volume
- 566
- Category
- Article
- ISSN
- 0022-328X
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The reported instances of inversion of configuration in the acid-catalyzed opening of cyclopropane rings are rare.2 The recent report' of exclusive inversion in the hydrogen chloride promoted opening of a fused cyclopropane ring prompts us to amplify our previous observations4 of a similarly strikin
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