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Volumn 58, Issue 39, 2002, Pages 7983-7986

An intramolecular Michael reaction strategy for the synthesis of 2,6-disubstituted-3-piperidinols

Author keywords

Diastereomeric piperidines; Intramolecular Michael reaction; Unsaturated amines

Indexed keywords

3 ACETOXY 6 ETHOXYCARBONYLMETHYL 2 METHYLPIPERIDINE; ACRYLIC ACID DERIVATIVE; ALANINE; PIPERIDINE DERIVATIVE; SULFONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037163334     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)00680-4     Document Type: Article
Times cited : (10)

References (37)
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    • Recent syntheses: (a) Pahl A., Wartchow R., Meyer H.H. Tetrahedron Lett. 39:1998;2095 (b) Agami C., Couty F., Mathieu H. Tetrahedron Lett. 39:1998;3505 (c) Yang C.-F., Xu Y.-M., Liao L.-X., Zhou W.-S. Tetrahedron Lett. 39:1998;9227 (d) Agami C., Couty F., Lam H., Mathieu H. Tetrahedron. 54:1998;8783 (e) Kiguchi T., Shirakawa M., Honda R., Ninomiya I., Naito T. Tetrahedron. 54:1998;15589 (f) Takahara H., Takahashi S., Kouno S., Momose T. J. Org. Chem. 63:1998;2224 (g) Ojima I., Vidal E.S. J. Org. Chem. 63:1998;7999 (h) Koulocheri S.D., Haroutounian S.A. Tetrahedron Lett. 40:1999;6869 (i) Yang C.-F., Liao L.-X., Xu Y.-M., Zhang H., Xia P., Zhou W.-S. Tetrahedron: Asymmetry. 10:1999;2311 (j) Toyooka N., Yoshida Y., Yotsui Y., Momose T. J. Org. Chem. 64:1999;4914 (k) Kirihara M., Nishio T., Yokoyama S., Kakuda H., Momose T. Tetrahedron. 55:1999;2911.
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    • 0033543535 scopus 로고    scopus 로고
    • Recent syntheses: (a) Pahl A., Wartchow R., Meyer H.H. Tetrahedron Lett. 39:1998;2095 (b) Agami C., Couty F., Mathieu H. Tetrahedron Lett. 39:1998;3505 (c) Yang C.-F., Xu Y.-M., Liao L.-X., Zhou W.-S. Tetrahedron Lett. 39:1998;9227 (d) Agami C., Couty F., Lam H., Mathieu H. Tetrahedron. 54:1998;8783 (e) Kiguchi T., Shirakawa M., Honda R., Ninomiya I., Naito T. Tetrahedron. 54:1998;15589 (f) Takahara H., Takahashi S., Kouno S., Momose T. J. Org. Chem. 63:1998;2224 (g) Ojima I., Vidal E.S. J. Org. Chem. 63:1998;7999 (h) Koulocheri S.D., Haroutounian S.A. Tetrahedron Lett. 40:1999;6869 (i) Yang C.-F., Liao L.-X., Xu Y.-M., Zhang H., Xia P., Zhou W.-S. Tetrahedron: Asymmetry. 10:1999;2311 (j) Toyooka N., Yoshida Y., Yotsui Y., Momose T. J. Org. Chem. 64:1999;4914 (k) Kirihara M., Nishio T., Yokoyama S., Kakuda H., Momose T. Tetrahedron. 55:1999;2911.
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    • Recent syntheses: (a) Pahl A., Wartchow R., Meyer H.H. Tetrahedron Lett. 39:1998;2095 (b) Agami C., Couty F., Mathieu H. Tetrahedron Lett. 39:1998;3505 (c) Yang C.-F., Xu Y.-M., Liao L.-X., Zhou W.-S. Tetrahedron Lett. 39:1998;9227 (d) Agami C., Couty F., Lam H., Mathieu H. Tetrahedron. 54:1998;8783 (e) Kiguchi T., Shirakawa M., Honda R., Ninomiya I., Naito T. Tetrahedron. 54:1998;15589 (f) Takahara H., Takahashi S., Kouno S., Momose T. J. Org. Chem. 63:1998;2224 (g) Ojima I., Vidal E.S. J. Org. Chem. 63:1998;7999 (h) Koulocheri S.D., Haroutounian S.A. Tetrahedron Lett. 40:1999;6869 (i) Yang C.-F., Liao L.-X., Xu Y.-M., Zhang H., Xia P., Zhou W.-S. Tetrahedron: Asymmetry. 10:1999;2311 (j) Toyooka N., Yoshida Y., Yotsui Y., Momose T. J. Org. Chem. 64:1999;4914 (k) Kirihara M., Nishio T., Yokoyama S., Kakuda H., Momose T. Tetrahedron. 55:1999;2911.
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    • Yang, C.-F.1    Liao, L.-X.2    Xu, Y.-M.3    Zhang, H.4    Xia, P.5    Zhou, W.-S.6
  • 13
    • 0033603564 scopus 로고    scopus 로고
    • Recent syntheses: (a) Pahl A., Wartchow R., Meyer H.H. Tetrahedron Lett. 39:1998;2095 (b) Agami C., Couty F., Mathieu H. Tetrahedron Lett. 39:1998;3505 (c) Yang C.-F., Xu Y.-M., Liao L.-X., Zhou W.-S. Tetrahedron Lett. 39:1998;9227 (d) Agami C., Couty F., Lam H., Mathieu H. Tetrahedron. 54:1998;8783 (e) Kiguchi T., Shirakawa M., Honda R., Ninomiya I., Naito T. Tetrahedron. 54:1998;15589 (f) Takahara H., Takahashi S., Kouno S., Momose T. J. Org. Chem. 63:1998;2224 (g) Ojima I., Vidal E.S. J. Org. Chem. 63:1998;7999 (h) Koulocheri S.D., Haroutounian S.A. Tetrahedron Lett. 40:1999;6869 (i) Yang C.-F., Liao L.-X., Xu Y.-M., Zhang H., Xia P., Zhou W.-S. Tetrahedron: Asymmetry. 10:1999;2311 (j) Toyooka N., Yoshida Y., Yotsui Y., Momose T. J. Org. Chem. 64:1999;4914 (k) Kirihara M., Nishio T., Yokoyama S., Kakuda H., Momose T. Tetrahedron. 55:1999;2911.
    • (1999) J. Org. Chem. , vol.64 , pp. 4914
    • Toyooka, N.1    Yoshida, Y.2    Yotsui, Y.3    Momose, T.4
  • 14
    • 0033525637 scopus 로고    scopus 로고
    • Recent syntheses: (a) Pahl A., Wartchow R., Meyer H.H. Tetrahedron Lett. 39:1998;2095 (b) Agami C., Couty F., Mathieu H. Tetrahedron Lett. 39:1998;3505 (c) Yang C.-F., Xu Y.-M., Liao L.-X., Zhou W.-S. Tetrahedron Lett. 39:1998;9227 (d) Agami C., Couty F., Lam H., Mathieu H. Tetrahedron. 54:1998;8783 (e) Kiguchi T., Shirakawa M., Honda R., Ninomiya I., Naito T. Tetrahedron. 54:1998;15589 (f) Takahara H., Takahashi S., Kouno S., Momose T. J. Org. Chem. 63:1998;2224 (g) Ojima I., Vidal E.S. J. Org. Chem. 63:1998;7999 (h) Koulocheri S.D., Haroutounian S.A. Tetrahedron Lett. 40:1999;6869 (i) Yang C.-F., Liao L.-X., Xu Y.-M., Zhang H., Xia P., Zhou W.-S. Tetrahedron: Asymmetry. 10:1999;2311 (j) Toyooka N., Yoshida Y., Yotsui Y., Momose T. J. Org. Chem. 64:1999;4914 (k) Kirihara M., Nishio T., Yokoyama S., Kakuda H., Momose T. Tetrahedron. 55:1999;2911.
    • (1999) Tetrahedron , vol.55 , pp. 2911
    • Kirihara, M.1    Nishio, T.2    Yokoyama, S.3    Kakuda, H.4    Momose, T.5
  • 21
    • 0033709712 scopus 로고    scopus 로고
    • For recent reviews on piperidine ring syntheses, see (a) Bailey P.D., Millwood P.A., Smith P.O. J. Chem. Soc., Chem. Commun. 633:1998; (b) Laschat S., Dickner T. Synthesis. 2000;1781.
    • (2000) Synthesis , pp. 1781
    • Laschat, S.1    Dickner, T.2


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