STERICALLY HINDERED 4-HYDROXYBENZENESULFENYL CHLORIDE: REACTIVITY WITH TRIVALENT PHOSPHORUS ESTERS

References

• Russ , C. R. and Douglass , I. B. 1971 . “ Chp. 8 ” . In Sulfur in Organic and Inorganic Chemistry , Edited by: Senning , A. Vol. 1 , New York : Marcel Dekker .
   Google Scholar
• Kuhle , E. 1971 . Synthesis , : 563
   Google Scholar
• Kuhle , E. 1971 . Synthesis , : 617
   Google Scholar
• Field , L. 1972 . Synthesis , : 101
   Google Scholar
• Field , L. 1978 . Synthesis , : 713
   Web of Science ®Google Scholar
• Hardstaff , W. H. and Langer , R. F. 1982 . “ Chp. 5 ” . In Sulfur in Organic and Inorganic Chemistry , Edited by: Senning , A. Vol. 4 , New York : Marcel Dekker . For reviews, see
   Google Scholar
• Kharasch , N. , Potempa , S. J. and Wehrmeister , A. 1946 . Chem. Rev. , 39 : 269
   PubMed Web of Science ®Google Scholar
• Langford , R. B. and Kharasch , N. 1958 . J. Org. Chem. , 23 : 1649
   Google Scholar
• Chang , L. L. , Denney , D. B. , Denney , D. Z. and Kazior , R. J. 1977 . J. Am. Chem. Soc. , 99 : 2293
   Web of Science ®Google Scholar
• Denney , D. B. , Denney , D. Z. and Gavrilovic , D. M. 1981 . Phosphorus Sulfur , 11 : 1
   Web of Science ®Google Scholar
• Green , T. W. 1981 . Protective Groups in Organic Synthesis , New York : Wiley-Interscience . For examples, see
   Google Scholar
• Meyers , C. Y. and Picciola , G. 1962 . Tetrahedron Lett. , : 971
   Google Scholar
• Cabiddu , S. , Ciuccatosta , F. , Cocco , M. T. , Loi , G. and Secci , M. 1977 . J. Heterocycl. Chem. , 14 : 123
   Google Scholar
• Wentrup , C. 1984 . Reactive Intermediates , 265 – 326 . Wiley-Interscience . For examples, see
   Google Scholar
• Yoshifuji , M. , Shima , I. , Inamoto , N. , Hirotsu , K. and Higuchi , T. 1981 . J. Am. Chem. Soc. , 103 : 4587
   Web of Science ®Google Scholar
• Niecke , E. and Ruger , R. 1983 . Angew. Chem., Int. Ed. Engl. , 22 : 155
   Web of Science ®Google Scholar
• Cowley , A. H. , Lasch , J. G. , Norman , N. C. , Pakulski , M. and Whittlesey , B. R. 1983 . J. Chem. Soc., Chem. Comm. , : 881
   Google Scholar
• Cowley , A. H. , Kilduff , J. E. , Norman , N. C. and Pakulski , M. 1983 . J. Am. Chem. Soc. , 105 : 4845
   Web of Science ®Google Scholar
• Yoshifuji , M. , Shibayama , K. , Inamoto , N. , Matsushita , T. and Nishimoto , K. 1983 . J. Am. Chem. Soc. , 105 : 2495
   Web of Science ®Google Scholar
• Yoshifuji , M. , Shima , I. , Shibayama , K. and Inamoto , N. 1984 . Tetrahedron lett. , 25 : 411
   Web of Science ®Google Scholar
• Pastor , S. D. 1984 . J. Org. Chem. , 49 : 5260
   Google Scholar
• Denney , D. B. and Moskal , M. A. 1974 . Phosphorus , 4 : 77
   Google Scholar
• Brintzinger , H. , Pfannstiel , K. , Koddebusch , H. and Kling , K. E. 1950 . Chem. Ber. , 83 : 87
   Google Scholar
• An equal volume of deuteriochloroform was added to provide a deuterium lock for the 1H NMR spectrometer
   Google Scholar
• Verkade , J. G. 1976 . Phosphorus Sulfur , 2 : 251
   Web of Science ®Google Scholar
• Vande Griend , L. J. , Verkade , J. G. , Pennings , J. F. M. and Buck , H. M. 1977 . J. Am. Chem. Soc. , 99 : 2459
   Web of Science ®Google Scholar
• Hodges , R. R. , Houle , F. A. , Beuchamp , J. L. , Montag , R. A. and Verkade , J. G. 1980 . J. Am. Chem. Soc. , 102 : 932
   Google Scholar
• Taira , K. and Gorenstein , D. G. 1984 . J. Am. Chem. Soc. , 106 : 7825
   Web of Science ®Google Scholar
• A quantity of 7 was isolated from the reaction mixture, mp 75–78°C; 1H NMR (CDCl3); δ 1.51 (s, C(CH3)3, 18 H), 5.64 (s, OH, 1 H), 7.10 (s, ArH, 2 H); MS: m/z 240 (M+). calcd. for C14H21ClO: C, 69.8; H, 8.8. Found: C, 69.9; H, 8.6
   Google Scholar
• Mayer , R. and Frey , H. J. 1964 . Angew. Chem. , 76 : 861
   Google Scholar