Facile Solid‐Phase Synthesis of Cycloalkylphosphonates and 1‐Cycloalkenylphosphonates Using Polymer‐Supported Phenylsulfonylmethylphosphonates

References

• Guillier , F. , Orain , D. and Bradley , M. 2000 . Chem. Rev. , 100 : 2091 Recent reviews on SPOS:
   PubMed Web of Science ®Google Scholar
• Sammelson , R. E. and Kurth , M. J. 2001 . Chem. Rev. , 101 : 137
   PubMed Web of Science ®Google Scholar
• Czarnik , A. W. 2001 . Solid‐Phase Organic Synthesis Vol. 1 , New York : Wiley .
   Google Scholar
• Nicolaou , K. C. , Hanko , R. and Hartwig , H. 2002 . Handbook of Combinatorial Chemistry Weinheim, , Germany : Wiley‐VCH .
   Google Scholar
• Dolle , R. E. 2002 . J. Comb. Chem. , 4 : 369
   PubMedGoogle Scholar
• Deprele , S. and Montchamp , J.‐L. 2001 . J. Org. Chem. , 66 : 5745 and references therein
   Google Scholar
• Sasse , K. 1964 . Methoden der Organischen Chemie (Houben‐Weyl) Edited by: Sasse , K. Vol. Band XII/1 , 294 – 337 . Stuttgart : Thieme . For example, phosphinic and phosphonic acid derivatives, phosphonochloridates, phosphine oxides, primary phosphines, and phosphonic acid derivatives, phosphonochloridates, phosphine oxides, primary phosphines, and dichlorophosphines. See
   Google Scholar
• Regitz , M. 1982 . Methodendeer Organischen Chemie (Houben‐Weyl) Vol. E2 , Stuttgart : Thieme .
   Google Scholar
• Frank , A. W. 1972 . Organic Phosphorus Compounds Edited by: Kosolapoff , G. M. and Maier , L. Vol. 4 , New York : Wiley . chap. 10
   Google Scholar
• Quin , L. D. 2000 . A Guide to Organophosphorus Chemistry New York : Wiley .
   Google Scholar
• Walker , B. J. 1997 . Organophosphorus Reagents in Organic Synthesis Edited by: Cadogan , J. I. G. New York : Academic Press . chap. 3
   Google Scholar
• Frank , A. W. 1961 . Chem. Rev. , 61 : 389
   Google Scholar
• Hoffmann , F. W. , Simmons , T. C. and Glunz III , L. J. 1957 . J. Am. Chem. Soc. , 79 : 3570 For selected examples of preparation of cycloalkylphosphonates, see
   Web of Science ®Google Scholar
• Callot , J. J. and Benezra , C. 1971 . Can. J. Chem. , 49 : 500
   Web of Science ®Google Scholar
• Yoneda , S. , Kawade , T. and Yoshida , Z. 1978 . J. Org. Chem. , 43 : 1980
   Web of Science ®Google Scholar
• Grandin , C. , Collignon , N. and Savignac , P. 1995 . Synthesis , : 239
   Google Scholar
• Jubault , P. , Feasson , C. and Collignon , N. 1996 . Tetrahedron Lett. , 37 : 3679
   Google Scholar
• Kim , D. Y. and Suh , K. H. 1998 . Synth. Commun. , 28 : 83
   Web of Science ®Google Scholar
• Han , L.‐B. , Mirzaei , F. , Zhao , C.-Q. and Tanaka , M. 2000 . J. Am. Chem. Soc. , 122 : 5407
   Web of Science ®Google Scholar
• Tayama , O. , Nakano , A. , Iwahama , T. , Sakaguchi , S. and Ishii , Y. 2004 . J. Org. Chem. , 69 : 5494
   PubMed Web of Science ®Google Scholar
• Shyaml , B. , Robert , E. and George , A. 1983 . Phosphorus, Sulfur Relat. Elem. , 15 : 15 For selected examples of preparation of 1-cycloalkenylphosphonates, see
   Google Scholar
• Kabachnik , M. M. , Novikora , Z. S. , Neganova , E. G. and Lutsenko , I. F. 1986 . Zh. Obshch. Khim. , 56 Zh. Obshch. Khim. 1986, 56, 781; J. Comb. Chem. Abstr. 1986, 105, 209043x.
   Google Scholar
• Fyles , T. M. and Leznoff , C. C. 1976 . Can J. Chem. , 54 : 935
   Web of Science ®Google Scholar
• Farrall , M. J. and Frechet , J. M. 1976 . J. Org. Chem. , 41 : 3877
   Web of Science ®Google Scholar
• Fyles , T. M. and Leznoff , C. C. 1978 . Can J. Chem. , 56 : 103
   Google Scholar
• Halm , C. , Evarts , J. and Kurth , M. J. 1997 . Tetrahedron Lett. , 38 : 7709
   Google Scholar
• Yamada , M. , Miyajima , T. and Horikawa , H. 1998 . Tetrahedron Lett. , 39 : 289
   Google Scholar
• Kulkarni , B. A. and Ganesan , A. 1999 . Tetrahedron Lett. , 40 : 5633
   Web of Science ®Google Scholar
• Cheng , W. C. , Halm , C. , Evarts , J. B. , Olmstead , M. M. and Kurth , M. J. 1999 . J. Org. Chem. , 64 : 8557
   Google Scholar
• Cheng , W. C. , Wong , M. , Olmstead , M. M. and Kurth , M. 2001 . J. Org. Chem. , 66 : 5528
   PubMed Web of Science ®Google Scholar
• Huang , W. , Cheng , S. and Sun , W. 2001 . Tetrahedron Lett. , 42 : 1973
   Web of Science ®Google Scholar
• Chen , Y. , Lam , Y. L. and Lee , S. Y. 2001 . Chem. Lett. , : 274
   Google Scholar
• Chen , Y. , Lam , Y. L. and Lai , Y. H. 2002 . Org. Lett. , 4 : 3935
   PubMed Web of Science ®Google Scholar
• Cheng , W. C. and Kurth , M. J. 2002 . J. Org. Chem. , 67 : 4387
   Google Scholar
• Cheng , W. C. , Wong , M. , Olmstead , M. M. and Kurth , M. J. 2002 . Org. Lett. , 4 : 741
   PubMed Web of Science ®Google Scholar
• Cheng , W. C. , Lin , C. C. and Kurth , M. J. 2002 . Tetrahedron Lett. , 43 : 2967
   Web of Science ®Google Scholar
• Cheng , Y. , Lam , Y. and Lai , Y. H. 2003 . Org. Lett. , 5 : 1067
   Google Scholar
• Kong , K.‐H. , Chen , Y. , Ma , X. , Chui , W. K. and Lam , Y. 2004 . J. Comb. Chem. , 6 : 928
   PubMedGoogle Scholar
• Li , W. , Chen , Y. and Lam , Y. L. 2004 . Tetrahedron Lett. , 45 : 6545
   Web of Science ®Google Scholar
• Li , W. and Lam , Y. L. 2005 . J. Comb. Chem. , 7 : 644
   PubMedGoogle Scholar
• Li , W. and Lam , Y. L. 2005 . J. Comb. Chem. , 7 : 721
   PubMed Web of Science ®Google Scholar
• Sheng , S.‐R. , Huang , P.‐G. , Zhou , W. , Luo , H.‐R. , Lin , S.‐Y. and Liu , X.‐L. 2004 . Synlett , : 2603
   Google Scholar
• Chen , S.‐H. , Horvath , R. F. , Joglar , J. , Fisher , M. J. and Danishefsky , S. J. 1991 . J. Org. Chem. , 56 : 5834
   Web of Science ®Google Scholar
• Graham , R. J. and Paquette , L. A. 1995 . J. Org. Chem. , 60 : 5770
   Google Scholar
• Lee , G. H. , Choi , E. B. , Lee , E. and Park , C. S. 1993 . Tetrahedron Lett. , 34 : 4541
   Web of Science ®Google Scholar