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Volumn 6, Issue 4, 2004, Pages 464-467

Preparation of poly(ethylene glycol) sulfonamide: Synthesis of N-supported β-aminoesters via the Aza-Baylis-Hillman reaction

Author keywords

[No Author keywords available]

Indexed keywords

ESTER DERIVATIVE; HETEROCYCLIC COMPOUND; POLY(ETHYLENE GLYCOL)SULFONAMIDE; POLYAMIDE; POLYSULFONE; SOLVENT; UNCLASSIFIED DRUG;

EID: 4143143021     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc049966n     Document Type: Article
Times cited : (32)

References (62)
  • 3
    • 4143079626 scopus 로고    scopus 로고
    • Enders, D., Noyori, R., Trost, B. M., Eds.; Thieme: Stuttgart; New York
    • (c) Kocienski, P. J. In Protecting Groups; Enders, D., Noyori, R., Trost, B. M., Eds.; Thieme: Stuttgart; New York, 2000, p 215-216.
    • (2000) Protecting Groups , pp. 215-216
    • Kocienski, P.J.1
  • 32
    • 0037127529 scopus 로고    scopus 로고
    • For the use of chiral sulfinimines, see: (h) Aggarwal, V. K.; Castro, A. M. M.; Mereu, A.; Adams, H. Tetrahedron Lett. 2002, 43, 1577-1581. (i) Shi, M.; Xu, Y. M. Tetrahedron: Asymmetry 2002, 13, 1195-1200. For the use of diphenylphosphinamide, see: (j) Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002, 43, 9171-9174. For reviews on the Baylis-Hillman reaction, see: (k) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062. (l) Ciganek, E. Org. React. 1997, 51, 201-350. (m) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 1577-1581
    • Aggarwal, V.K.1    Castro, A.M.M.2    Mereu, A.3    Adams, H.4
  • 33
    • 0037150594 scopus 로고    scopus 로고
    • For the use of chiral sulfinimines, see: (h) Aggarwal, V. K.; Castro, A. M. M.; Mereu, A.; Adams, H. Tetrahedron Lett. 2002, 43, 1577-1581. (i) Shi, M.; Xu, Y. M. Tetrahedron: Asymmetry 2002, 13, 1195-1200. For the use of diphenylphosphinamide, see: (j) Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002, 43, 9171-9174. For reviews on the Baylis-Hillman reaction, see: (k) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062. (l) Ciganek, E. Org. React. 1997, 51, 201-350. (m) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 1195-1200
    • Shi, M.1    Xu, Y.M.2
  • 34
    • 0037049187 scopus 로고    scopus 로고
    • For the use of chiral sulfinimines, see: (h) Aggarwal, V. K.; Castro, A. M. M.; Mereu, A.; Adams, H. Tetrahedron Lett. 2002, 43, 1577-1581. (i) Shi, M.; Xu, Y. M. Tetrahedron: Asymmetry 2002, 13, 1195-1200. For the use of diphenylphosphinamide, see: (j) Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002, 43, 9171-9174. For reviews on the Baylis-Hillman reaction, see: (k) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062. (l) Ciganek, E. Org. React. 1997, 51, 201-350. (m) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 9171-9174
    • Shi, M.1    Zhao, G.-L.2
  • 35
    • 0342419508 scopus 로고    scopus 로고
    • For the use of chiral sulfinimines, see: (h) Aggarwal, V. K.; Castro, A. M. M.; Mereu, A.; Adams, H. Tetrahedron Lett. 2002, 43, 1577-1581. (i) Shi, M.; Xu, Y. M. Tetrahedron: Asymmetry 2002, 13, 1195-1200. For the use of diphenylphosphinamide, see: (j) Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002, 43, 9171-9174. For reviews on the Baylis-Hillman reaction, see: (k) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062. (l) Ciganek, E. Org. React. 1997, 51, 201-350. (m) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (1996) Tetrahedron , vol.52 , pp. 8001-8062
    • Basavaiah, D.1    Rao, P.D.2    Hyma, R.S.3
  • 36
    • 0000892247 scopus 로고    scopus 로고
    • For the use of chiral sulfinimines, see: (h) Aggarwal, V. K.; Castro, A. M. M.; Mereu, A.; Adams, H. Tetrahedron Lett. 2002, 43, 1577-1581. (i) Shi, M.; Xu, Y. M. Tetrahedron: Asymmetry 2002, 13, 1195-1200. For the use of diphenylphosphinamide, see: (j) Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002, 43, 9171-9174. For reviews on the Baylis-Hillman reaction, see: (k) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062. (l) Ciganek, E. Org. React. 1997, 51, 201-350. (m) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (1997) Org. React. , vol.51 , pp. 201-350
    • Ciganek, E.1
  • 37
    • 0037366617 scopus 로고    scopus 로고
    • For the use of chiral sulfinimines, see: (h) Aggarwal, V. K.; Castro, A. M. M.; Mereu, A.; Adams, H. Tetrahedron Lett. 2002, 43, 1577-1581. (i) Shi, M.; Xu, Y. M. Tetrahedron: Asymmetry 2002, 13, 1195-1200. For the use of diphenylphosphinamide, see: (j) Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002, 43, 9171-9174. For reviews on the Baylis-Hillman reaction, see: (k) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062. (l) Ciganek, E. Org. React. 1997, 51, 201-350. (m) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (2003) Chem. Rev. , vol.103 , pp. 811-891
    • Basavaiah, D.1    Rao, A.J.2    Satyanarayana, T.3
  • 44
    • 4143049533 scopus 로고    scopus 로고
    • note
    • 13C NMR.
  • 48
    • 0037029830 scopus 로고    scopus 로고
    • For examples, see: (a) Genski, T.; Taylor, R. J. K. Tetrahedron Lett. 2002, 43, 3573-3576. (b) Anand, R. V.; Baktharaman, S.; Singh, V. K. Tetrahedron Lett. 2002, 43, 5393-5395. (c) Jauch, J. Eur. J. Org. Chem. 2001, 473-476. (d) Keck, G. E.; Welch, D., S. Org. Lett. 2002, 4, 3687-90.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 3573-3576
    • Genski, T.1    Taylor, R.J.K.2
  • 49
    • 0037194197 scopus 로고    scopus 로고
    • For examples, see: (a) Genski, T.; Taylor, R. J. K. Tetrahedron Lett. 2002, 43, 3573-3576. (b) Anand, R. V.; Baktharaman, S.; Singh, V. K. Tetrahedron Lett. 2002, 43, 5393-5395. (c) Jauch, J. Eur. J. Org. Chem. 2001, 473-476. (d) Keck, G. E.; Welch, D., S. Org. Lett. 2002, 4, 3687-90.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 5393-5395
    • Anand, R.V.1    Baktharaman, S.2    Singh, V.K.3
  • 50
    • 0035141019 scopus 로고    scopus 로고
    • For examples, see: (a) Genski, T.; Taylor, R. J. K. Tetrahedron Lett. 2002, 43, 3573-3576. (b) Anand, R. V.; Baktharaman, S.; Singh, V. K. Tetrahedron Lett. 2002, 43, 5393-5395. (c) Jauch, J. Eur. J. Org. Chem. 2001, 473-476. (d) Keck, G. E.; Welch, D., S. Org. Lett. 2002, 4, 3687-90.
    • (2001) Eur. J. Org. Chem. , pp. 473-476
    • Jauch, J.1
  • 51
    • 0037126262 scopus 로고    scopus 로고
    • For examples, see: (a) Genski, T.; Taylor, R. J. K. Tetrahedron Lett. 2002, 43, 3573-3576. (b) Anand, R. V.; Baktharaman, S.; Singh, V. K. Tetrahedron Lett. 2002, 43, 5393-5395. (c) Jauch, J. Eur. J. Org. Chem. 2001, 473-476. (d) Keck, G. E.; Welch, D., S. Org. Lett. 2002, 4, 3687-90.
    • (2002) Org. Lett. , vol.4 , pp. 3687-3690
    • Keck, G.E.1    Welch, D.S.2
  • 60
    • 0034853422 scopus 로고    scopus 로고
    • For reactions on close structures, see, for example: (g) Huck, J.; Receveur, J.-M.; Roumestant, M.-L.; Martinez, J. Synlett 2001, 1467-1469. (h) Huck, J.; Duru, C.; Roumestant, M. L.; Martinez, J. Synthesis 2003, 2165-2168. (i) Varray, S.; Lazaro, R.; Martinez, J.; Lamaty, F. Organometallics 2003, 22, 2426-2435.
    • (2001) Synlett , pp. 1467-1469
    • Huck, J.1    Receveur, J.-M.2    Roumestant, M.-L.3    Martinez, J.4
  • 61
    • 0142120603 scopus 로고    scopus 로고
    • For reactions on close structures, see, for example: (g) Huck, J.; Receveur, J.-M.; Roumestant, M.-L.; Martinez, J. Synlett 2001, 1467-1469. (h) Huck, J.; Duru, C.; Roumestant, M. L.; Martinez, J. Synthesis 2003, 2165-2168. (i) Varray, S.; Lazaro, R.; Martinez, J.; Lamaty, F. Organometallics 2003, 22, 2426-2435.
    • (2003) Synthesis , pp. 2165-2168
    • Huck, J.1    Duru, C.2    Roumestant, M.L.3    Martinez, J.4
  • 62
    • 0037899511 scopus 로고    scopus 로고
    • For reactions on close structures, see, for example: (g) Huck, J.; Receveur, J.-M.; Roumestant, M.-L.; Martinez, J. Synlett 2001, 1467-1469. (h) Huck, J.; Duru, C.; Roumestant, M. L.; Martinez, J. Synthesis 2003, 2165-2168. (i) Varray, S.; Lazaro, R.; Martinez, J.; Lamaty, F. Organometallics 2003, 22, 2426-2435.
    • (2003) Organometallics , vol.22 , pp. 2426-2435
    • Varray, S.1    Lazaro, R.2    Martinez, J.3    Lamaty, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.