Asymmetric palladium-catalyzed hydroarylation of styrenes and dienes
SM Podhajsky, Y Iwai, A Cook-Sneathen, MS Sigman
Index: Podhajsky, Susanne M.; Iwai, Yasumasa; Cook-Sneathen, Amanda; Sigman, Matthew S. Tetrahedron, 2011 , vol. 67, # 24 p. 4435 - 4441
Full Text: HTML
Citation Number: 22
Abstract
Alkenes are desirable and highly versatile starting materials for organic transformations, and well-known substrates for palladium catalysis. Typically, these reactions result in the formation of a new alkene product via β-hydride elimination. In contrast to this scenario, our laboratory has been involved in the development of alkene hydro-and difunctionalization reactions, where β-hydride elimination can be controlled. We report herein the ...
Related Articles:
A New Class of Non??Racemic Chiral Macrocycles: A Conformational and Synthetic Study
[Gibson, Susan E.; Mainolfi, Nello; Kalindjian, S. Barret; Wright, Paul T.; White, Andrew J. P. Chemistry - A European Journal, 2005 , vol. 11, # 1 p. 69 - 80]
Catalytic enantioselective Steglich rearrangements using chiral N-heterocyclic carbenes
[Campbell, Craig D.; Concellon, Carmen; Smith, Andrew D. Tetrahedron Asymmetry, 2011 , vol. 22, # 7 p. 797 - 811]