Addition of sulphenyl halides to alkenyl-metal compounds: III. Arenesulphenyl chloride additions to triethoxy-and triphenylvinylsilanes and to triphenylvinylgermanium. …
RA Howie, GM Spencer, JL Wardell, JN Low
文献索引：Howie, R. Alan; Spencer, Gavin M.; Wardell, James L. Journal of Organometallic Chemistry, 1992 , vol. 437, # 1/2 p. 111 - 125
Abstract Additions of arenesulphenyl chlorides (eg ArSCI p-XC 6 H 4 SCl; X Me or Cl; 4-Y- 2-O 2 NC 6 H 4 SCl; Y H, Me or NO 2) to R 3 MCH CH 2 [R 3 M Ph 3 Si,(EtO) 3 Si or Ph 3 Ge] can provide both possible adducts: R 3 MCHSArCH 2 Cl (the anti-Markovnikov adducts) and R 3 MCHClCH 2 SAr (the Markovnikov adducts). In reactions in CH 2 Cl 2 at room temperature, the former adducts always dominate (> 77%) and can be the exclusive ...
