- Studies toward the generation of functionalized quaternary carbon centers relying on wittig and wittig-still allylic ether anionic transpositions
-
Although the [2,3]-Wittig and Wittig-Still rearrangements have long been known, their application in the generation of quaternary carbon centers in carbocyclic ring systems is sparse. Model studies utilizing this strategy and possible mechanisms are discussed herein. Unprecedented examples of an α-elimination pathway from stannylmethyl allyl ethers as a major undesired product in some Wittig-Still rearrangements are reported.
- Hanessian, Stephen,Dorich, Stephane,Chattopadhyay, Amit Kumar,Bueschleb, Martin
-
p. 8915 - 8921
(2013/09/24)
-
- Intramolecular Photocycloaddition of the 3-(3-Butenyloxy)-2-cyclohexenone System
-
The irradiation of 5,5-dimethyl-3-(4-methyl-3-pentenyloxy)-2-cyclohexenone gave regioselectively, 6,6,10,10-tetramethyl-2-oxatricyclo1,5>undecan-8-one, while, that of 5,5-dimethyl-3--2-cyclohexenone afforded, regio- and stereoselectively, 1,5,5-trimethyl-8-oxatetracyclo2,7.01,5>tetradecan-3-one.
- Umehara, Takashi,Inouye, Yoshinobu,Kakisawa, Hiroshi
-
p. 3492 - 3494
(2007/10/02)
-