55546-61-7Relevant articles and documents
Sulfonium Ylides by (3+2) Cycloaddition of Arynes with Vinyl Sulfides: Stereoselective Synthesis of Highly Substituted Alkenes
Li, Yuanming,Mück-Lichtenfeld, Christian,Studer, Armido
supporting information, p. 14435 - 14438 (2016/11/11)
The reaction of in situ generated arynes with vinyl sulfides provides benzannulated sulfonium ylides in a (3+2) cycloaddition. Trapping of the intermediate ylides with electrophiles (proton transfer or a second aryne addition) and subsequent β-elimination give rise to di-, tri-, or tetrasubstituted alkenes with high stereoselectivity. Experimental studies and DFT calculations provide insight into the mechanisms of these cascade reactions.
Palladium-catalyzed thioesterirication of alkynes with O-methyl S-phenyl thiocarbonate
Hua,Takeda,Onozawa,Abe,Tanaka
, p. 2899 - 2900 (2007/10/03)
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Experimental and Theoretical Study of the Radical-Chain Addition of Benzenethiol to Heterosubstituted Allenes
Pasto, Daniel J.,L'Hermine, Gael
, p. 685 - 694 (2007/10/02)
The radical-chain addition of benzenethiol to phenylallene (PHA), methoxyallene (MEOA), carbomethoxyallene (CBA), cyanoallene (CNA), chloroallene (ClA), and (phenylthio)- and allene (PHSA and MPHSA) has been studied.In all cases, exc