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Volumn 10, Issue , 2014, Pages 1383-1389

Asymmetric Ugi 3CR on isatin-derived ketimine: Synthesis of chiral 3,3-disubstituted 3-aminooxindole derivatives

Author keywords

Isatin; Multicomponent; Oxindole; Peptidomimetics; Ugi

Indexed keywords


EID: 84904089314     PISSN: None     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.10.141     Document Type: Article
Times cited : (34)

References (43)
  • 1
    • 84869188848 scopus 로고    scopus 로고
    • doi:10.1021/cr300135y
    • Singh, G. S.; Desta, Z. Y. Chem. Rev. 2012, 112, 6104-6155. doi:10.1021/cr300135y
    • (2012) Chem. Rev , vol.112 , pp. 6104-6155
    • Singh, G.S.1    Desta, Z.Y.2
  • 5
    • 34547575038 scopus 로고    scopus 로고
    • Nonpeptidic ligands for peptide-activated G protein-coupled receptors
    • DOI 10.1021/cr050984g
    • Blakeney, J. S.; Reid, R. C.; Le, G. T.; Fairlie, D. P. Chem. Rev. 2007, 107, 2960-3041. doi:10.1021/cr050984g (Pubitemid 47189009)
    • (2007) Chemical Reviews , vol.107 , Issue.7 , pp. 2960-3041
    • Blakeney, J.S.1    Reid, R.C.2    Le, G.T.3    Fairlie, D.P.4
  • 7
    • 43049146180 scopus 로고    scopus 로고
    • Non-peptide arginine-vasopressin antagonists: The vaptans
    • DOI 10.1016/S0140-6736(08)60695-9, PII S0140673608606959
    • Decaux, G.; Soupart, A.; Vassart, G. Lancet 2008, 371, 1624-1632. doi:10.1016/S0140-6736(08)60695-9 (Pubitemid 351626846)
    • (2008) The Lancet , vol.371 , Issue.9624 , pp. 1624-1632
    • Decaux, G.1    Soupart, A.2    Vassart, G.3
  • 8
    • 33746214558 scopus 로고    scopus 로고
    • 1B receptor antagonist, SSR149415, in a social interaction test in rats
    • DOI 10.1016/j.ejphar.2006.06.032, PII S0014299906006583
    • Shimazaki, T.; Iijima, M.; Chaki, S. Eur. J. Pharmacol. 2006, 543, 63-67. doi:10.1016/j.ejphar.2006.06.032 (Pubitemid 44092711)
    • (2006) European Journal of Pharmacology , vol.543 , Issue.1-3 , pp. 63-67
    • Shimazaki, T.1    Iijima, M.2    Chaki, S.3
  • 21
    • 84862175237 scopus 로고    scopus 로고
    • doi:10.1021/cr100233r
    • Dömling, A.; Wang, W.; Wang, K. Chem. Rev. 2012, 112, 3083-3135. doi:10.1021/cr100233r
    • (2012) Chem. Rev , vol.112 , pp. 3083-3135
    • Dömling, A.1    Wang, W.2    Wang, K.3
  • 22
    • 2542509173 scopus 로고    scopus 로고
    • doi:10.1002/1521-3773(20000915)39:18〈3168::AID-ANIE3168〉3.0. CO;2-U
    • Dömling, A.; Ugi, I. Angew. Chem., Int. Ed. 2000, 39, 3168-3210. doi:10.1002/1521-3773(20000915)39:18〈3168::AID-ANIE3168〉3.0.CO;2-U
    • (2000) Angew. Chem., Int. Ed , vol.39 , pp. 3168-3210
    • Dömling, A.1    Ugi, I.2
  • 24
    • 79953203183 scopus 로고    scopus 로고
    • doi:10.1021/jo102305q
    • Santra, S.; Andreana, P. R. J. Org. Chem. 2011, 76, 2261-2264. doi:10.1021/jo102305q
    • (2011) J. Org. Chem , vol.76 , pp. 2261-2264
    • Santra, S.1    Andreana, P.R.2
  • 27
    • 55749094321 scopus 로고    scopus 로고
    • 3-carbonyl compounds: Effective synthesis of -trifluoromethyl amino acid derivatives
    • DOI 10.1016/j.tet.2008.10.004, PII S0040402008017766
    • Gulevich, A. V.; Shevchenko, N. E.; Balenkova, E. S.; Röschenthaler, G.-V.; Nenajdenko, V. G. Tetrahedron 2008, 64, 11706-11712. doi:10.1016/j.tet.2008.10.004 (Pubitemid 50318655)
    • (2008) Tetrahedron , vol.64 , Issue.51 , pp. 11706-11712
    • Gulevich, A.V.1    Shevchenko, N.E.2    Balenkova, E.S.3    Roschenthaler, G.-V.4    Nenajdenko, V.G.5
  • 28
    • 33646562788 scopus 로고    scopus 로고
    • The Ugi reaction with 2-substituted cyclic imines. Synthesis of substituted proline and homoproline derivatives
    • DOI 10.1016/j.tet.2006.04.021, PII S0040402006006181
    • Nenajdenko, V. G.; Gulevich, A. V.; Balenkova, E. S. Tetrahedron 2006, 62, 5922-5930. doi:10.1016/j.tet.2006.04.021 (Pubitemid 43728082)
    • (2006) Tetrahedron , vol.62 , Issue.25 , pp. 5922-5930
    • Nenajdenko, V.G.1    Gulevich, A.V.2    Balenkova, E.S.3
  • 31
    • 17144366282 scopus 로고    scopus 로고
    • doi:10.1002/anie.200460548
    • Ram, D. J.; Yus, M. Angew. Chem., Int. Ed. 2005, 44, 1602-1634. doi:10.1002/anie.200460548
    • (2005) Angew. Chem., Int. Ed , vol.44 , pp. 1602-1634
    • Ram, D.J.1    Yus, M.2
  • 33
    • 12344268639 scopus 로고    scopus 로고
    • A novel highly selective chiral auxiliary for the asymmetric synthesis of L-and D-amino acid derivatives via a multicomponent ugi reaction
    • DOI 10.1021/jo048389m
    • Basso, A.; Banfi, L.; Riva, R.; Guanti, G. J. Org. Chem. 2005, 70, 575-579. doi:10.1021/jo048389m (Pubitemid 40129420)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.2 , pp. 575-579
    • Basso, A.1    Banfi, L.2    Riva, R.3    Guanti, G.4
  • 35
    • 0034678615 scopus 로고    scopus 로고
    • doi:10.1002/(SICI)1521-3773(20000417)39:8〈1431::AID-ANIE1431〉3. 0.CO;2-N
    • Oertel, K.; Zech, G.; Kunz, H. Angew. Chem., Int. Ed. 2000, 39, 1431-1433. doi:10.1002/(SICI)1521-3773(20000417)39:8〈1431::AID- ANIE1431〉3. 0.CO;2-N
    • (2000) Angew. Chem., Int. Ed , vol.39 , pp. 1431-1433
    • Oertel, K.1    Zech, G.2    Kunz, H.3
  • 36
    • 0037157803 scopus 로고    scopus 로고
    • Stereoselective U-4CRs with 1-amino-5-desoxy-5-thio-2,3,4-O-isobutanoyl- D-xylopyranose-An effective and selectively removable chiral auxiliary
    • DOI 10.1016/S0040-4020(02)00484-2, PII S0040402002004842
    • Ross, G. F.; Herdtweck, E.; Ugi, I. Tetrahedron 2002, 58, 6127-6133. doi:10.1016/S0040-4020(02)00484-2 (Pubitemid 35245192)
    • (2002) Tetrahedron , vol.58 , Issue.30 , pp. 6127-6133
    • Ross, G.F.1    Herdtweck, E.2    Ugi, I.3
  • 37
    • 0003439281 scopus 로고    scopus 로고
    • Farrugia, L. J.: University of Glasgow, Scotland
    • ORTEP-3 for Windows; Farrugia, L. J.: University of Glasgow, Scotland, 1997.
    • (1997) ORTEP-3 for Windows


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.