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2
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(b) Rosen, M. K.; Schreiber, S. L. Angew. Chem., Int. Ed. Engl. 1992, 31, 384, and references cited therein.
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Rosen, M.K.1
Schreiber, S.L.2
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3
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0025893168
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(a)
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(a) Liu, J.; Farmer, J. D.; Lane, W. S.; Friedman, J.; Weissman, I.; Schreiber, S. L. Cell 1991, 66, 807.
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Cell
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Liu, J.1
Farmer, J.D.2
Lane, W.S.3
Friedman, J.4
Weissman, I.5
Schreiber, S.L.6
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4
-
-
0026753687
-
-
(b)
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(b) Liu, J.; Albers, M. W.; Wandless, T. L.; Luan, S.; Alberg, D. G.; Belshaw, P. J.; Cohen, P.; Mackintosh, C.; Klee, C. B.; Schreiber, S. L. Biochemistry 1992, 31, 3896.
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Liu, J.1
Albers, M.W.2
Wandless, T.L.3
Luan, S.4
Alberg, D.G.5
Belshaw, P.J.6
Cohen, P.7
Mackintosh, C.8
Klee, C.B.9
Schreiber, S.L.10
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5
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0028202076
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Lyons, W. E.; George, E. B.; Dawson, T. M.; Steiner, J. P.; Snyder, S. H. Proc. Natl. Acad. Sci. USA 1994, 91, 3191.
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Lyons, W.E.1
George, E.B.2
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6
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0028352763
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Gold, B.G.1
Storm-Dickerson, T.2
Austin, D.R.3
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9
-
-
84991430718
-
-
All compounds were characterized by satisfying proton NMR, MS and HRMS. Carbon-13 NMR spectra of some of the compounds were also recorded when necessary for structure assignment
-
All compounds were characterized by satisfying proton NMR, MS and HRMS. Carbon-13 NMR spectra of some of the compounds were also recorded when necessary for structure assignment.
-
-
-
-
10
-
-
0029087036
-
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Chrystal, E. J. T.; Couper, L.; Robins, D. J. Tetrahedron 1995, 51, 10241.
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Tetrahedron
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Chrystal, E.J.T.1
Couper, L.2
Robins, D.J.3
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12
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0029970519
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Jones, K.; Newton, R. F.; Christopher, J. Y. Tetrahedron 1996, 52, 4133.
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(1996)
Tetrahedron
, vol.52
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-
Jones, K.1
Newton, R.F.2
Christopher, J.Y.3
-
14
-
-
84991415508
-
-
Upon scale-up, intermediate 4 was prepared from crude 3 in quantitative yield. No purification is necessary for transformations from 1 to 4 besides routine workups
-
Upon scale-up, intermediate 4 was prepared from crude 3 in quantitative yield. No purification is necessary for transformations from 1 to 4 besides routine workups.
-
-
-
-
15
-
-
0021215623
-
-
(a)
-
(a) Hiemstra, H.; Fortgens, H. P.; Speckamp, W. N. Tetrahedron Lett. 1984, 25, 3115.
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, pp. 3115
-
-
Hiemstra, H.1
Fortgens, H.P.2
Speckamp, W.N.3
-
19
-
-
84991423008
-
-
Although the stereochemistry of 6 was assigned by NOE experiments on 14β (major), it is not crucial for our synthesis of the targets
-
Although the stereochemistry of 6 was assigned by NOE experiments on 14β (major), it is not crucial for our synthesis of the targets.
-
-
-
-
20
-
-
84991426228
-
-
Resolution of the two enantiomers of the amines similar to 18 is being actively pursued
-
Resolution of the two enantiomers of the amines similar to 18 is being actively pursued.
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