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1
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0000716787
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Nucleophilic Addition to Imines and Imine Derivatives
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Schreiber S.L. (Ed), Pergamon, Oxford Part 1
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Volkmann R.A. Nucleophilic Addition to Imines and Imine Derivatives. In: Schreiber S.L. (Ed). Comprehensive Organic Synthesis: Additions to C-X π-Bonds Vol. 1 (1991), Pergamon, Oxford 355-396 Part 1
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(1991)
Comprehensive Organic Synthesis: Additions to C-X π-Bonds
, vol.1
, pp. 355-396
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Volkmann, R.A.1
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6
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65949113523
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Selected examples: Cortistatin A
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Selected examples: Cortistatin A:
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7
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33644946432
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Indolizomycin:
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Aoki S., Watanabe Y., Sanagawa M., Setiawan A., Kotoku N., and Kobayashi M. J. Am. Chem. Soc. 128 (2006) 3148 Indolizomycin:
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(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 3148
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Aoki, S.1
Watanabe, Y.2
Sanagawa, M.3
Setiawan, A.4
Kotoku, N.5
Kobayashi, M.6
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8
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0021920250
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Rivastigmine:
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Yamashita F., Hotta K., Kurasawa S., Okami Y., and Umezawa H. J. Antibiot. 38 (1985) 58 Rivastigmine:
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(1985)
J. Antibiot.
, vol.38
, pp. 58
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Yamashita, F.1
Hotta, K.2
Kurasawa, S.3
Okami, Y.4
Umezawa, H.5
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10
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65949116283
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For phosphoramidite-type ligands, see
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For phosphoramidite-type ligands, see:
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19
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65949112834
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Me-DuPHOS(O) is now commercially available from Aldrich (CAS 638132-66-8, no. 678635).
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Me-DuPHOS(O) is now commercially available from Aldrich (CAS 638132-66-8, no. 678635).
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20
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0033521210
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Yamada K.-I., Harwood S.J., Gröger H., and Shibasaki M. Angew. Chem., Int. Ed. 38 (1999) 3504
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(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 3504
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Yamada, K.-I.1
Harwood, S.J.2
Gröger, H.3
Shibasaki, M.4
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26
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65949109608
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For benzotriazole adducts, see
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For benzotriazole adducts, see:
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27
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13844266386
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For sulfinic acid adducts, see:
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Katritzky A.R., Manju K., Singh S.K., and Meher N.K. Tetrahedron 61 (2005) 2555; For sulfinic acid adducts, see:
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(2005)
Tetrahedron
, vol.61
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Katritzky, A.R.1
Manju, K.2
Singh, S.K.3
Meher, N.K.4
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48
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15044340854
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One report mentions the use of isopropyl ester:
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One report mentions the use of isopropyl ester:. Akullian L.C., Porter J.R., Traverse J.F., Snapper M.L., and Hoveyda A.H. Adv. Synth. Catal. 347 (2005) 417
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(2005)
Adv. Synth. Catal.
, vol.347
, pp. 417
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Akullian, L.C.1
Porter, J.R.2
Traverse, J.F.3
Snapper, M.L.4
Hoveyda, A.H.5
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53
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0347601837
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Davies A.S., Gates N.J., Lindsay K.B., Tang M., and Pyne S.G. Synlett (2004) 49
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(2004)
Synlett
, pp. 49
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Davies, A.S.1
Gates, N.J.2
Lindsay, K.B.3
Tang, M.4
Pyne, S.G.5
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56
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34247582194
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The same strategy has also been used recently by:
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The same strategy has also been used recently by:. Kamimura A., Okawa H., Morisaki Y., Ishikawa S., and Uno H. J. Org. Chem. 72 (2007) 3569
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(2007)
J. Org. Chem.
, vol.72
, pp. 3569
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Kamimura, A.1
Okawa, H.2
Morisaki, Y.3
Ishikawa, S.4
Uno, H.5
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57
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33749114652
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Ono N., Matsumoto K., Ogawa T., Tani H., and Uno H. J. Chem. Soc., Perkin Trans. 1 (1996) 1905
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(1996)
J. Chem. Soc., Perkin Trans. 1
, pp. 1905
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Ono, N.1
Matsumoto, K.2
Ogawa, T.3
Tani, H.4
Uno, H.5
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61
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0032572845
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This additive has been used by Knochel in the catalytic asymmetric alkylation of aldehydes:
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This additive has been used by Knochel in the catalytic asymmetric alkylation of aldehydes:. Lutz C., Graf C.D., and Knochel P. Tetrahedron 54 (1998) 10317
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(1998)
Tetrahedron
, vol.54
, pp. 10317
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Lutz, C.1
Graf, C.D.2
Knochel, P.3
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62
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65949097389
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note
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R=10.3 min).
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72
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34848874183
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Arisawa M., Terada Y., Takahashi K., Nakagawa N., and Nishida A. Chem. Rec. 7 (2007) 238
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(2007)
Chem. Rec.
, vol.7
, pp. 238
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Arisawa, M.1
Terada, Y.2
Takahashi, K.3
Nakagawa, N.4
Nishida, A.5
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76
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0023865490
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Gannett P.M., Nagel D.L., Reilly P.J., Lawson T., Sharpe J., and Toth B. J. Org. Chem. 53 (1988) 1064
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(1988)
J. Org. Chem.
, vol.53
, pp. 1064
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Gannett, P.M.1
Nagel, D.L.2
Reilly, P.J.3
Lawson, T.4
Sharpe, J.5
Toth, B.6
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77
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0342826148
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Hibino S., Sugino E., Adachi Y., Nomi K., and Sato K. Heterocycles 28 (1989) 275
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(1989)
Heterocycles
, vol.28
, pp. 275
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Hibino, S.1
Sugino, E.2
Adachi, Y.3
Nomi, K.4
Sato, K.5
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78
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0842289640
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Kurono N., Honda E., Komatsu F., Orito K., and Tokuda M. Tetrahedron 60 (2004) 1791
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(2004)
Tetrahedron
, vol.60
, pp. 1791
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Kurono, N.1
Honda, E.2
Komatsu, F.3
Orito, K.4
Tokuda, M.5
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