By Barry Martin Trost; Ian Fleming, chimiste.; Stuart L Schreiber
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Extra info for Comprehensive organic synthesis : selectivity, strategy & efficiency in modern organic chemistry / volume 1, Additions to C-X [pi]-bonds, part 1 / ed. Stuart L. Schreiber
Des, J. Am. Chem. , 1972,94,4555. 29. For intermediate (8) see ref. 1; for intermediate (9) see ref. 136; and for an intermediate analogous to (11)see ref. 141. 30. See refs 12 and 14. 31. See ref. 9. 32. (a) D. Mootz, A. Zinnius and B. Bottcher, Angew. , 1969, 81, 398 (MSINLI); (b) R. D. Rogers, J. L. Atwood and R. Gruning, J. Organornet. , 1978,157,229 (TMSIAL). 33. (a) D. R. Armstrong, D. Barr, W. Clegg, R. E. Mulvey, D. Reed, R. Snaith and K. Wade, J. Chem. , Chem. , 1986, 869 (DOKBOU); (b) D.
Wilhelm, T. Clark and P. von R. Schleyer, Angew. , Int. Ed. , 1984,23, 621 (COKSEA, COKSEAIO). 148. See ref 21e. 149. P. G. Williard and J. M. Salvino, J . Chem. ,Chem. , 1986, 153 (DILPUJ). 150. P. Berno, C. Floriani, A. Chiesi-Villa and C. Guastini, Organometallics, 1990,9, 1995. 151. D. Seebach, R. Amstutz, T. Laube, W. B. Schweizer and J. D. Dunitz, J . Am. Chem. , 1985, 107, 5403 (DEDXEP, DEDXIT, DEDXOZ). 152. P. G. Williard and M. J. Hintze, J. Am. Chem. , 1990, 112, 8602. 153. J. Dekker, J.
L. Gumby and H. D. Zook,J . Org. , 1959,24,709, (d) H. D. Zook, W. L. Kelly and I. Y. Posey, J. Org. , 1%8, 33, 3477; (e) A. G. Pinkus, J. G. Lindberg and A. B. Wu, J. Chem. , Chem. , 1969, 1350; 1970, 859; ( f ) G. E. Coates, J. A. Heslop, M. E. Redwood and D. D. Ridley, J. Chem. SOC. A, 1968, 1118; (g) E. Weiss, H. Alsdorf and H. Kuhr. Angew. , Int. Ed. , 1967, 6, 801; (h) see also ref. 20c. 22. See ref 21e. 23. (a) H. 0. , Benjamin, Menlo Park, New York, 1972, p. J. le Noble and H. F. Moms, J.