Protonation of (2-formylnorbornadiene)cyclopentadienylrhodium.First example of direct transition metal participation in stabilizing of α-carbocationic centre in O-protonated acyl-substituted π-complexes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
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1. Rhodium;Comprehensive Organometallic Chemistry II;1995
2. NMR studies of some η4-diene-rhodium(I) and main group metal derivatives of funtionally substituted cyclopentadienes;Journal of Organometallic Chemistry;1989-04
3. Highly diastereofacial selective chelation of a phosphite-containing .alpha.,.beta.-unsaturated ketone system to the Fe(CO)2 group;Journal of the American Chemical Society;1988-07
4. Cationic hydroxyallylolefin rhodium complexes [Rh(η2, 3-C7H6-3-R-2-CR1OH)(η5-Cp)]+PF6− (R, R1 = H, Alk, Cp = C5H5, C5H4Me, C5Me5) with intramolecular O-H ⋯ Rh hydrogen bonds. Formation of {[CpRh(η2, 3-C7H6-3-R-2-CR1OH)]2-F2POO}+PF6− dimers as a result of partial hydrolysis of the PF6− anion;Journal of Organometallic Chemistry;1988-01
5. Cationic products from O-protonation reaction of 2-acylnorbornadiene complexes of rhodium with hydrogen chloride in ether: structure, reactivity and nature of hydrogen bond;Journal of Organometallic Chemistry;1987-11
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