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1
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0032583448
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(a) Kong, F.; Zhao, N.; Siegel, M. M.; Janota, K.; Ashcroft, J. S.; Koehn, F. E.; Borders, D. B.; Carter, G. T. J. Am. Chem. Soc. 1998, 120, 13301.
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Kong, F.1
Zhao, N.2
Siegel, M.M.3
Janota, K.4
Ashcroft, J.S.5
Koehn, F.E.6
Borders, D.B.7
Carter, G.T.8
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2
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0033452947
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(b) Shi, S. D.-H.; Hendrickson, C. L.; Marshall, A. G.; Siegel, M. M.; Kong, F.; Carter, G. T. J. Am. Soc. Mass. Spectrom. 1999, 10, 1285.
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J. Am. Soc. Mass. Spectrom.
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Shi, S.D.-H.1
Hendrickson, C.L.2
Marshall, A.G.3
Siegel, M.M.4
Kong, F.5
Carter, G.T.6
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3
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0033931843
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Singh, M. P.; Petersen, P. J.; Weiss, W. J.; Kong, F.; Greenstein, M. Antimicrob. Agents Chemother. 2000, 44, 2154.
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Antimicrob. Agents Chemother.
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Singh, M.P.1
Petersen, P.J.2
Weiss, W.J.3
Kong, F.4
Greenstein, M.5
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4
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27144508724
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see the Supporting Information
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(a) Compounds 4a and 4b were prepared by Wadsworth-Emmons olefmation of the corresponding 3-protected derivative of 3,4-dihydroxybenzaldehyde (see the Supporting Information).
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5
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0034609172
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(b) 4c: Gu, W.; Jing, X.; Pan, X.; Chan, A. S. C.; Yang, T.-K. Tetrahedron Lett. 2000, 41, 6079.
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(2000)
Tetrahedron Lett.
, vol.41
, pp. 6079
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Gu, W.1
Jing, X.2
Pan, X.3
Chan, A.S.C.4
Yang, T.-K.5
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8
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27144539114
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This unpublished work was conducted by Dr. Minglang Wu
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This unpublished work was conducted by Dr. Minglang Wu.
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9
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0343416938
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Chiappe, C.; LoMoro, G.; Munforte, P. Tetrahedron 1997, 53, 10471.
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Tetrahedron
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Chiappe, C.1
Lomoro, G.2
Munforte, P.3
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10
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85047695069
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For acetonide protection in the presence of an aryl PMB-ether, see: Trost, B. M.; Dudash, J., Jr.; Dirat, O. Chem. Eur. J. 2002, 8, 259.
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Chem. Eur. J.
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Trost, B.M.1
Dudash Jr., J.2
Dirat, O.3
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11
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0001021477
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(a) Felix, A. M.; Heimer, E. P.; Lambros, T. J.; Tzougraki, C.; Meienhofer, J. J. Org. Chem. 1978, 21, 4194.
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Felix, A.M.1
Heimer, E.P.2
Lambros, T.J.3
Tzougraki, C.4
Meienhofer, J.5
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13
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0032784301
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(c) Kawada, T.; Asano, R.; Hayashida, S.; Sakuno, T. J. Org. Chem. 1999, 64, 9268.
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Kawada, T.1
Asano, R.2
Hayashida, S.3
Sakuno, T.4
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14
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0000443519
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(a) Park, M. H.; Takeda, R.; Nakanishi, K. Tetrahedron Lett. 1987, 28, 3823.
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(1987)
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Park, M.H.1
Takeda, R.2
Nakanishi, K.3
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15
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0030605827
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(b) Rodebaugh, R.; Debenham, J. S.; Fraser-Reid, B. Tetrahedron Lett. 1996, 37, 5477.
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Rodebaugh, R.1
Debenham, J.S.2
Fraser-Reid, B.3
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17
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27144507283
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note
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Attempted introduction of taurine by other methods, such as dehydrative carbodiimide coupling of the carboxylic acid or acylation of the corresponding acid chloride, were unsuccessful.
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18
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27144509276
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note
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13C NMR spectra of 3.
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19
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27144535882
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note
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The optical rotation data (unpublished) was graciously provided by Dr. Fangming Kong. In a private communication, he notes some uncertainty with the magnitude of the rotations measured in his work, but the sign of the rotation of 3 derived from naturally occurring saccharomicin is consistently negative.
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20
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0034630891
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(a) McDonald, F. E.; Reddy, K. S., Díaz, Y. J. Am. Chem. Soc. 2000, 122, 4304.
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McDonald, F.E.1
Reddy, K.S.2
Díaz, Y.3
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21
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0035476321
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(b) McDonald, F. E.; Reddy, K. S. Angew. Chem., Int. Ed. 2001, 40, 3653.
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McDonald, F.E.1
Reddy, K.S.2
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