Cyclopropanation of Vinyl Sulfides and Vinyl Sulfones

References

• Parham , W. E. and Schweizer , E. E. 1963 . Org. React. , 13 : 55 – 90 . For reviews, see, Dave, V.; Warnhoff, E.W. Org. React. (1970) 18, 217–401
   Google Scholar
• Parham , W. E. , Kajigaeshi , S. and Groen , S. H. 1972 . Bull. Chem. Soc. Japan , 45 : 509 – 512 .
   Google Scholar
• Kositikov , R. R. 1980 . Izv. Akad. Nauk USSR Ser, Ser. Khim. , : 1354 – 1358 .
   Google Scholar
• Simmons , H. E. and Smith , R. D. 1959 . J. Am. Chem. Soc. , 81 : 4256 For reviews, see Simmons, H.E.; Cairns, T.L.; Vladuchick, S.A.; Hoineas, C.M. Org. React. (1973) 20, 1–131; Furukawa, J.; Kawabata, N. Adv. Organomet. Chem. (1974) 12, 83–134
   Web of Science ®Google Scholar
• Christil , M. and Brunn , E. 1981 . Angew. Chem. Int. Ed. , 20 : 850
   Google Scholar
• Suda , M. 1981 . Synthesis , : 714 Vorbruggen, H.; Kottwitz, J. Synthesis (1975) 636
   Google Scholar
• Fedorynski , M. 1977 . Synthesis , : 783
   Google Scholar
• Weyerstahl , P. , Blume , G. and Muller , C. 1972 . Tetrahedron Lett. , : 3869
   Google Scholar
• Shostakovski , S. M. , Nikolski , N. S. and Makosza , M. 1974 . Tezisy Dokl. Nauchn. Sess. Khim. Tekhnol. Org. Soedin. Ser. Sernistykh Neftei , : 144 ref. CA. 85, 176884K
   Google Scholar
• Prilezhaeva , E. P. , Petukyhova , N. P. and Shostakovskii , M. F. 1962 . Dokl. Akad. Nauk SSSR , 144 : 1059 – 1061 . This compound was reported to have a mp of 55–6°c. Chem. Abstr. (1962) 57, 136321
   Google Scholar