(Matrix presented) We describe a new, straightforward, and easy-to-handle method for achieving an unprecedented trimethylsilyl halide-catalyzed Michaelis-Arbuzov-like rearrangement. This rearrangement occurs at temperatures from room temperature to 80°C and does not require addition of any alkyl halide. The scope and limitations of this new reaction are explored, as well as its mechanism.
Renard, Pierre-Yves,Vayron, Philippe,Mioskowski, Charles
p. 1661 - 1664
(2007/10/03)
INFLUENCE OF THE CHARACTER OF THE ESTER RING ON THE STABILITY OF 2,2-(ALKYLENEDIOXY)-1,2λ5-OXAPHOSPHOL-4-ENES
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Ragulin, V. V.,Petrov, A. A.,Zakharov, V. I.,Razumova, N. A.
p. 646 - 652
(2007/10/02)
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