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Roques, B.P.7
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2
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5644279954
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Bláha, K.1
Farag, A.M.2
Van Der Helm, D.3
Hossain, M.B.4
Budešínský, M.5
Malon, P.6
Smolíková, J.7
Tichý, M.8
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3
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Eisler, K.; Rudinger, J.; Šorm, F. Coll. Czech. Chem. Commun. 1966, 31, 4563.
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Eisler, K.1
Rudinger, J.2
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4
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0000832282
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For the reductive cleavage of the corresponding azlactone, see: a) Ali, M.; Khan, N. H.; Siddiqui, A. A. Synth. Commun. 1976, 6, 227. Via a Wittig reaction, see:
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Ali, M.1
Khan, N.H.2
Siddiqui, A.A.3
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6
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6544282676
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c) Rudman, D.; Merister, A.; Greenstein, J. P. J. Am. Chem. Soc. 1952, 74, 551.
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8
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a) Pauly, R.; Sasaki, N. A.; Potier, P. Tetrahedron Lett. 1994, 35, 237.
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Pauly, R.1
Sasaki, N.A.2
Potier, P.3
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10
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85038132189
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Ref. 2 and 3c
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a) Ref. 2 and 3c.
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11
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0031779863
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For the amidocarbonylation of cyclohexanecarboxaldehyde, followed by an acylase catalysed enantioselective hydrolysis, see: b) Beller, M.; Eckert, M.; Geissler, H.; Napierski, B.; Rebenstock, H.; Holla, E. W. Chem. Eur. J. 1998, 4, 935.
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Chem. Eur. J.
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Beller, M.1
Eckert, M.2
Geissler, H.3
Napierski, B.4
Rebenstock, H.5
Holla, E.W.6
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14
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0017339896
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b) Johnston, T. P.; McCaleb, G. S.; Clayton, S. D.; Frye, J. L.; Krauth, C. A.; Montgomery, J. A. J. Med. Chem. 1977, 20, 279.
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Johnston, T.P.1
McCaleb, G.S.2
Clayton, S.D.3
Frye, J.L.4
Krauth, C.A.5
Montgomery, J.A.6
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15
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0019920627
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For reduction of the N-methyl amino derivative, see ref. 1a
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b) Harris, C. M.; Harris, T. M. J. Am. Chem. Soc. 1982, 104, 363. For reduction of the N-methyl amino derivative, see ref. 1a.
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J. Am. Chem. Soc.
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Harris, C.M.1
Harris, T.M.2
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17
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85038138699
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In our hands, hydrogenation of (S)-2 with Pt/C in aqueous HCl afforded a greenish solution and large amounts of catalyst were needed for the reaction to reach completion
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In our hands, hydrogenation of (S)-2 with Pt/C in aqueous HCl afforded a greenish solution and large amounts of catalyst were needed for the reaction to reach completion.
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18
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85038143293
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European Patent Application 0 823 416 A1, 1998
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Sato, T.; Honda, Y.; Izawa, K. (Ajinomoto Co., Inc.), European Patent Application 0 823 416 A1, 1998.
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Sato, T.1
Honda, Y.2
Izawa, K.3
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19
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85038137401
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a ref 1b
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a) ref 1b.
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20
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85038135282
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(Novartis Corp.) USP 5,770,624, 1998
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b) Parker, D. T. (Novartis Corp.) USP 5,770,624, 1998.
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Parker, D.T.1
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21
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0008451370
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Hayashi, T.; Konishi, M.; Fukushima, M.; Kanehira, K.; Hioki, T.; Kumada, M. J. Org. Chem. 1983, 48, 2195.
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Hayashi, T.1
Konishi, M.2
Fukushima, M.3
Kanehira, K.4
Hioki, T.5
Kumada, M.6
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23
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0001038169
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b) Riley, D. P.; Shumate, R. E. J. Org. Chem. 1980, 45, 5187. See also the hydrogenation of 1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid in:
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J. Org. Chem.
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Riley, D.P.1
Shumate, R.E.2
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24
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6544244513
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c) Rapala, R. T.; Lavagnino, E. R.; Shepard, E. R.; Farkas, E. J. Am. Chem. Soc. 1957, 79, 3770.
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Rapala, R.T.1
Lavagnino, E.R.2
Shepard, E.R.3
Farkas, E.4
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25
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85038140945
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Analysis of the mother liquor showed that 1% of cyclohexaneacetic acid had been formed, so the reaction has a selectivity of 99%
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Analysis of the mother liquor showed that 1% of cyclohexaneacetic acid had been formed, so the reaction has a selectivity of 99%.
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26
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85038149423
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The catalyst was re-used without loss of activity
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The catalyst was re-used without loss of activity.
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