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1
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85030198287
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Summer intern participant in the Purdue University Quest Fellowship Program
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Summer intern participant in the Purdue University Quest Fellowship Program.
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2
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0026527430
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Robertson, D. W.; Lacefield, W. B.; Bloomquist, W.; Pfeifer, W.; Simon, R. L.; Cohen, M. L. J. Med. Chem. 1992, 35, 310-319.
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(1992)
J. Med. Chem.
, vol.35
, pp. 310-319
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Robertson, D.W.1
Lacefield, W.B.2
Bloomquist, W.3
Pfeifer, W.4
Simon, R.L.5
Cohen, M.L.6
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4
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0001105678
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(a) Archer, S.; Lewis, T. R.; Unser, M. J. J. Am. Chem. Soc. 1957, 79, 4194-4198.
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(1957)
J. Am. Chem. Soc.
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Archer, S.1
Lewis, T.R.2
Unser, M.J.3
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6
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85030209860
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note
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Ratios were obtained by capillary gas chromatography CAM Capillary column (15 m × 0.5 m I.D.). GC measurements were performed on a Hewlett-Packard 5200 GC instrument equipped with a flame ionization detector (FID) and a Hewlett-Packard electronic integrator. The carrier gas (helium) flow rate is 1 mL/rnin. with a 20:1 split ratio. The oven temperature is increased from 100°C to 220°C over 30 minutes.
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10
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0001803662
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Trost, B. M., Ed.; Pergamon: New York
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(d) For a review on the reduction of imines see: Hutchins, R. O.; Hutchins, M. K. In Comprehensive Organic Synthesis: Selectivity, Strategy and Efficiency in Modern Organic Chemistry, Trost, B. M., Ed.; Pergamon: New York. 1991; Vol. 8, pp 25-78.
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(1991)
Comprehensive Organic Synthesis: Selectivity, Strategy and Efficiency in Modern Organic Chemistry
, vol.8
, pp. 25-78
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Hutchins, R.O.1
Hutchins, M.K.2
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11
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21344485033
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(e) For a review of diastereoselective and enantioselective reduction of imines see: Zhu, Q.-C.; Hutchins, R. O.; Hutchins, M. K. Org. Prep. Proced. Int. 1994, 26, 193-236.
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(1994)
Org. Prep. Proced. Int.
, vol.26
, pp. 193-236
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Zhu, Q.-C.1
Hutchins, R.O.2
Hutchins, M.K.3
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12
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4043071644
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(a) Borch, R. F.; Bernstein, M. D.; Durst, H. D. J. Am. Chem. Soc. 1971, 93, 2897-2904.
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(1971)
J. Am. Chem. Soc.
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, pp. 2897-2904
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Borch, R.F.1
Bernstein, M.D.2
Durst, H.D.3
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14
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0027161303
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Yoon, N. M.; Kim, E. G.; Son, H. S.; Choi, J. Synth. Commun. 1993, 23, 1595-1599.
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(1993)
Synth. Commun.
, vol.23
, pp. 1595-1599
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Yoon, N.M.1
Kim, E.G.2
Son, H.S.3
Choi, J.4
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15
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33845551193
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Hutchins, R. O.; Su, W.-Y.; Sivakumar, R.; Cistone, F.; Stercho, Y. P. J. Org. Chem. 1983, 48, 3412-3422.
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(1983)
J. Org. Chem.
, vol.48
, pp. 3412-3422
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Hutchins, R.O.1
Su, W.-Y.2
Sivakumar, R.3
Cistone, F.4
Stercho, Y.P.5
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16
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0025142350
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(a) Abdel-Magid, A. F.; Maryanoff, C. A.; Carson, K. G. Tetrahedron Lett. 1990, 31, 5595-5598.
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(1990)
Tetrahedron Lett.
, vol.31
, pp. 5595-5598
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Abdel-Magid, A.F.1
Maryanoff, C.A.2
Carson, K.G.3
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18
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0000473171
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(a) Marchini, P.; Liso, G.; Reho, A.; Liberatore, F.; Moracci, F. M. J. Org. Chem. 1975, 40, 3453-3456.
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(1975)
J. Org. Chem.
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Marchini, P.1
Liso, G.2
Reho, A.3
Liberatore, F.4
Moracci, F.M.5
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19
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84985701326
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(b) Gribble, G. W.; Jasinski, J. M.; Pellicone, J. T.; Panetta, J. A. Synthesis 1978, 766-768.
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(1978)
Synthesis
, pp. 766-768
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Gribble, G.W.1
Jasinski, J.M.2
Pellicone, J.T.3
Panetta, J.A.4
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22
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85030198702
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note
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The reagent prepared from (±)-ethylhexanoic acid could also be a mixture of diastereomers.
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23
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85030200372
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note
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4) and concentrated. The crude amine product was either hydrogenolyzed (5% Pd/C) to remove the benzyl group or isolated as an HCl salt by the addition of anhydrous HCl.
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