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For example, see: (a) 11-membered analogues: Kirst, H. A.; Wind, J. A.; Paschal, J. W. J. Org. Chem. 1987, 52, 4359.
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0001315691
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(b) 12-Membered analogues: Kibwage, I. O.; Busson, R.; Janssen, G.; Hoogmartens, J.; Vanderhaeghe H.; Brache J. J. Org. Chem. 1987, 52, 990.
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Brache, J.6
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(c) 13-Membered analogues: Burnell-Curty, C.; Faghih, R.; Pagano, T.; Henry, R. F.; Lartey, P. A. J. Org. Chem. 1996, 61, 5153.
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(d) 14-Membered azalide: Jones, A. B. J. Org. Chem. 1992, 57, 4361.
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Bright, G. M.; Nagel, A. A.; Bordner, J.; Desai, K. A.; Dibrino, J. N.; Nowakowska, J.; Vincent, L.; Watrous, R. W.; Sciavolino, F. C.; English, A. R.; Retsema, J. A.; Anderson, M. R.; Brennan, L. A.; Borovoy, R. J.; Cimochowaski, C. R.; Faiella, J. A.; Girard, D.; Herbert, C.; Manousos, M.; Mason, R. J. Antibiot. 1988, 41, 1029.
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Sciavolino, F.C.9
English, A.R.10
Retsema, J.A.11
Anderson, M.R.12
Brennan, L.A.13
Borovoy, R.J.14
Cimochowaski, C.R.15
Faiella, J.A.16
Girard, D.17
Herbert, C.18
Manousos, M.19
Mason, R.20
more..
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15
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0016720108
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(b) Slawinski, W.; Bojarska-Dahlig, H.; Glabski, T.; Dziegielewska, I.; Biedrzycki, M.; Naperty, S.; Rec, J. R. Nether. Chem. Soc. 1975, 94, 236.
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Naperty, S.6
Rec, J.R.7
Nether8
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Flynn, E. H.; Murphy, H. W.; McMahon, R. E. J. Am. Chem. Soc. 1955, 77, 3104-3105.
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Flynn, E.H.1
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McMahon, R.E.3
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18
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12244289231
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Unpublished results from these laboratories
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Yasukata, T.; Narukawa, Y. Unpublished results from these laboratories. This method for Cbz-protection of the cladinosyl moiety of erythromycin derivatives was originally invented.
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Yasukata, T.1
Narukawa, Y.2
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19
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Baskaran, S.; Islam, I.; Raghavan, S.; Chandrasekaran, S. Chem. Lett. 1987, 1175.
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(b) Wilkening, R. R.; Ratcliffe, R. W.; Doss, G. A.; Mosley, R. T.; Ball, R. G. Tetrahedron, 1997, 53, 16923.
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Ball, R.G.5
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23
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12244291861
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-
note
-
X-ray crystal structures and crystal data for 13a and 13b are reported in the Supporting Information.
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-
-
-
24
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0032757367
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For basic hydrolysis of 11,12-cyclic carbonate of erythromycin analogues, see: (a) Faghih, R.; Burnell-Curty, C.; Lartey, P. A.; Peterson, A.; Klein, L. L.; Bennani, Y. L.; Nellans, H. N. Eur. J. Med. Chem. 1999, 34 (3), 261.
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Lartey, P.A.3
Peterson, A.4
Klein, L.L.5
Bennani, Y.L.6
Nellans, H.N.7
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27
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0000708236
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Silverman, G. S.; Rakita, P. E., Ed.; Marcel Dekker: New York
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Cannon, K. C.; Know, G. R. In Handbook of Grignard Reagents; Silverman, G. S.; Rakita, P. E., Ed.; Marcel Dekker: New York, 1996; pp 497-526.
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Cannon, K.C.1
Know, G.R.2
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28
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12244249815
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note
-
MICs (minimum inhibitory concentrations) were determined by NCCLS (National Committee for Clinical Laboratory Standards) recommended microbroth dilution methods using cation-adjusted Mueller Hinton broth (Difco Laboratories, Detroit, MI).
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