Carbon-carbon bond formation by induced elimination from unsymmetrically substituted (allyl)(allyl') palladium complexes

A Goliaszewski, J Schwartz

Index: Goliaszewski, Alan; Schwartz, Jeffrey Journal of the American Chemical Society, 1984 , vol. 106, # 17 p. 5028 - 5030

Full Text: HTML

Citation Number: 66

Abstract

" Unidentified C. material.* Oxidant added to MeCN solution of bis (ally1) at-30 OC. CIonic medium 0.1 M Bu4NBF, in MeCN; reference electrode Ag, AgCi; Pt working electrode;-30 OC. taneous reductive elimination from these complexes does not occur; alkyl groupsubstituted allylic complexes decompose by processes involving hydride transfer^.^ Reductive elimination of 1, 4-dienes from (73-allyl)(7$ alkenyl) palladium (II) species can ...

Related Articles:

Weakening C− O Bonds: Ti (III), a New Reagent for Alcohol Deoxygenation and Carbonyl Coupling Olefination

[Barrero, Alejandro F.; Herrador, M. Mar; Quilez Del Moral, Jose F.; Arteaga, Pilar; Arteaga, Jesus F.; Dieguez, Horacio R.; Sanchez, Elena M. Journal of Organic Chemistry, 2007 , vol. 72, # 8 p. 2988 - 2995]

On the regioselectivity of coupling of substituted allyl radicals. Steric versus FMO control

[Pasto, Daniel J.; L'Hermine, Gael Tetrahedron, 1993 , vol. 49, # 16 p. 3259 - 3272]

On the regioselectivity of coupling of substituted allyl radicals. Steric versus FMO control

[Pasto, Daniel J.; L'Hermine, Gael Tetrahedron, 1993 , vol. 49, # 16 p. 3259 - 3272]

Radikal??Stabilisierungsenergie–das MMEVBH??Kraftfeld

[Roth, Wolfgang R.; Staemmler, Volker; Neumann, Martin; Schmuck, Carsten Liebigs Annalen, 1995 , # 6 p. 1061 - 1118]

More Articles...