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Volumn 3, Issue 5, 2001, Pages 404-406

A "Double Random" Strategy for the Preparation of Saponin Libraries

Author keywords

[No Author keywords available]

Indexed keywords

DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; GLUCOSE; SAPONIN;

EID: 0035461107     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc010014g     Document Type: Article
Times cited : (23)

References (30)
  • 11
    • 0004108162 scopus 로고
    • Cambridge University Press: Cambridge, U.K.
    • (a) Hosttetmann, K.; Marston, A. Saponins; Cambridge University Press: Cambridge, U.K., 1995.
    • (1995) Saponins
    • Hosttetmann, K.1    Marston, A.2
  • 22
    • 0001472774 scopus 로고    scopus 로고
    • It has been reported that glycosylation with rhamnopyranosyl donor 17 under the promotion of NIS/HOTf produced the corresponding α-glycosides dominantly (if not exclusively) because of its strong anomeric effect. See the following. (a) Duynstee, H. I.; van Vliet, M. J.; van der Marel, G. A.; van Boom, J. H. Eur. J. Org. Chem. 1998, 303-307. (b) Douglas, N. L.; Ley, S. V.; Lucking, U.; Warriner, S. L. J. Chem. Soc., Perkin Tran. 1 1998, 51-66. Lu, S.-F.; O'yang, Q.; Guo, Z.-W.; Yu, B.; Hui, Y. J. Org. Chem. 1997, 62, 8400-8405. Ley, S. V.; Priepke, H. W. M. Angew. Chem., Int. Ed. Engl. 1994, 33, 2292-2294.
    • (1998) Eur. J. Org. Chem. , pp. 303-307
    • Duynstee, H.I.1    Van Vliet, M.J.2    Van Der Marel, G.A.3    Van Boom, J.H.4
  • 23
    • 33748601612 scopus 로고    scopus 로고
    • It has been reported that glycosylation with rhamnopyranosyl donor 17 under the promotion of NIS/HOTf produced the corresponding α-glycosides dominantly (if not exclusively) because of its strong anomeric effect. See the following. (a) Duynstee, H. I.; van Vliet, M. J.; van der Marel, G. A.; van Boom, J. H. Eur. J. Org. Chem. 1998, 303-307. (b) Douglas, N. L.; Ley, S. V.; Lucking, U.; Warriner, S. L. J. Chem. Soc., Perkin Tran. 1 1998, 51-66. Lu, S.-F.; O'yang, Q.; Guo, Z.-W.; Yu, B.; Hui, Y. J. Org. Chem. 1997, 62, 8400-8405. Ley, S. V.; Priepke, H. W. M. Angew. Chem., Int. Ed. Engl. 1994, 33, 2292-2294.
    • (1998) J. Chem. Soc., Perkin Tran. 1 , pp. 51-66
    • Douglas, N.L.1    Ley, S.V.2    Lucking, U.3    Warriner, S.L.4
  • 24
    • 0031442147 scopus 로고    scopus 로고
    • It has been reported that glycosylation with rhamnopyranosyl donor 17 under the promotion of NIS/HOTf produced the corresponding α-glycosides dominantly (if not exclusively) because of its strong anomeric effect. See the following. (a) Duynstee, H. I.; van Vliet, M. J.; van der Marel, G. A.; van Boom, J. H. Eur. J. Org. Chem. 1998, 303-307. (b) Douglas, N. L.; Ley, S. V.; Lucking, U.; Warriner, S. L. J. Chem. Soc., Perkin Tran. 1 1998, 51-66. Lu, S.-F.; O'yang, Q.; Guo, Z.-W.; Yu, B.; Hui, Y. J. Org. Chem. 1997, 62, 8400-8405. Ley, S. V.; Priepke, H. W. M. Angew. Chem., Int. Ed. Engl. 1994, 33, 2292-2294.
    • (1997) J. Org. Chem. , vol.62 , pp. 8400-8405
    • Lu, S.-F.1    O'Yang, Q.2    Guo, Z.-W.3    Yu, B.4    Hui, Y.5
  • 25
    • 33748597918 scopus 로고
    • It has been reported that glycosylation with rhamnopyranosyl donor 17 under the promotion of NIS/HOTf produced the corresponding α-glycosides dominantly (if not exclusively) because of its strong anomeric effect. See the following. (a) Duynstee, H. I.; van Vliet, M. J.; van der Marel, G. A.; van Boom, J. H. Eur. J. Org. Chem. 1998, 303-307. (b) Douglas, N. L.; Ley, S. V.; Lucking, U.; Warriner, S. L. J. Chem. Soc., Perkin Tran. 1 1998, 51-66. Lu, S.-F.; O'yang, Q.; Guo, Z.-W.; Yu, B.; Hui, Y. J. Org. Chem. 1997, 62, 8400-8405. Ley, S. V.; Priepke, H. W. M. Angew. Chem., Int. Ed. Engl. 1994, 33, 2292-2294.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2292-2294
    • Ley, S.V.1    Priepke, H.W.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.