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Volumn 20, Issue 5, 2015, Pages 8574-8582

Highly diastereoselective synthesis of spiropyrazolones

Author keywords

Cascade Reaction; Diastereoselective; Spiropyrazolones

Indexed keywords

AMINE; PYRAZOLONE DERIVATIVE; SPIRO COMPOUND;

EID: 84938360628     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules20058574     Document Type: Article
Times cited : (16)

References (12)
  • 1
    • 84855913892 scopus 로고    scopus 로고
    • Enantioselective methodologies for the synthesis of spiro compounds
    • Rios, R. Enantioselective methodologies for the synthesis of spiro compounds. Chem. Soc. Rev 2012, 41, 1060-1074.
    • (2012) Chem. Soc. Rev , vol.41 , pp. 1060-1074
    • Rios, R.1
  • 2
    • 58149185277 scopus 로고    scopus 로고
    • Spiro skeletons: A class of privileged structure for chiral ligand design
    • Ding, K.; Han, Z.; Wang, Z. Spiro skeletons: A class of privileged structure for chiral ligand design. Chem. Asian J. 2009, 4, 32-41.
    • (2009) Chem. Asian J , vol.4 , pp. 32-41
    • Ding, K.1    Han, Z.2    Wang, Z.3
  • 3
    • 70349784950 scopus 로고    scopus 로고
    • Targeting structural and stereochemical complexity by organocascade catalysis: Construction of spirocyclic oxindoles having multiple stereocenters
    • Bencivenni, G.; Wu, L.; Mazzanti, A.; Giannichi, B.; Pesciaioli, F.; Song, M.; Bartoli, G.; Melchiorre, P. Targeting Structural and Stereochemical Complexity by Organocascade Catalysis: Construction of Spirocyclic Oxindoles Having Multiple Stereocenters. Angew. Chem. Int. Ed. 2009, 48, 7200-7203.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 7200-7203
    • Bencivenni, G.1    Wu, L.2    Mazzanti, A.3    Giannichi, B.4    Pesciaioli, F.5    Song, M.6    Bartoli, G.7    Melchiorre, P.8
  • 4
    • 77956458174 scopus 로고    scopus 로고
    • Organocatalytic synthesis of spiro compounds via a cascade Michael-Michael-Aldol reaction
    • Companyo, X.; Zea, A.; Alba, A.N.R.; Mazzanti, A.; Moyano, A.; Rios, R. Organocatalytic synthesis of spiro compounds via a cascade Michael-Michael-Aldol reaction. Chem. Commun. 2010, 46, 6953-6955.
    • (2010) Chem. Commun , vol.46 , pp. 6953-6955
    • Companyo, X.1    Zea, A.2    Alba, A.N.R.3    Mazzanti, A.4    Moyano, A.5    Rios, R.6
  • 5
    • 84882411324 scopus 로고    scopus 로고
    • Organocatalytic diastereo-And enantioselective 1, 3-dipolar cycloaddition of azlactones and methyleneindolinones
    • Sun, W.; Zhu, G.; Wu, C.; Li, G.; Hong, L.; Wang, R. Organocatalytic diastereo-And enantioselective 1, 3-dipolar cycloaddition of azlactones and methyleneindolinones. Angew. Chem. Int. Ed. 2013, 52, 8633-8637.
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 8633-8637
    • Sun, W.1    Zhu, G.2    Wu, C.3    Li, G.4    Hong, L.5    Wang, R.6
  • 6
    • 80052833054 scopus 로고    scopus 로고
    • Enantioselective michael/cyclization reaction sequence: Scaffold-inspired synthesis of spirooxindoles with multiple stereocenters
    • Cao, Y.; Jiang, X.; Liu, L.; Shen, F.; Zhang, F.; Wang, R. Enantioselective Michael/Cyclization Reaction Sequence: Scaffold-Inspired Synthesis of Spirooxindoles with Multiple Stereocenters. Angew. Chem. Int. Ed. 2011, 50, 9124-9127.
    • (2011) Angew. Chem. Int. Ed , vol.50 , pp. 9124-9127
    • Cao, Y.1    Jiang, X.2    Liu, L.3    Shen, F.4    Zhang, F.5    Wang, R.6
  • 7
    • 84889084575 scopus 로고    scopus 로고
    • Enantioselective organocatalytic synthesis of sulfur-containing spirocyclic compounds
    • Geant, P. Urban, M.; Remes, M.; Cisarova, I.; Vesely, J. Enantioselective organocatalytic synthesis of sulfur-containing spirocyclic compounds. Eur. J. Org. Chem. 2013, 7979-7988.
    • (2013) . Eur. J. Org. Chem , pp. 7979-7988
    • Geant Urban P, M.1    Remes, M.2    Cisarova, I.3    Vesely, J.4
  • 8
    • 84901386874 scopus 로고    scopus 로고
    • Asymmetric synthesis of spiropyrazolones through phosphine-catalyzed [4+1] annulation
    • Han, X.; Yao, W.; Wang, T.; Tan, Y.R.; Yan, Z.; Kwiatkowski, J.; Lu, Y. Asymmetric synthesis of spiropyrazolones through phosphine-catalyzed [4+1] annulation. Angew. Chem. Int. Ed. 2014, 53, 5643-547.
    • (2014) Angew. Chem. Int. Ed , vol.53 , pp. 5643-6547
    • Han, X.1    Yao, W.2    Wang, T.3    Tan, Y.R.4    Yan, Z.5    Kwiatkowski, J.6    Lu, Y.7
  • 9
    • 84902081011 scopus 로고    scopus 로고
    • Stereocontrolled construction of six vicinal stereogenic centers on spiropyrazolones via organocascade michael/michael/1, 2-Addition reactions
    • Chauhan, P.; Mahajan, S.; Loh, C.C.J.; Raabe, G.; Enders, D. Stereocontrolled Construction of Six Vicinal Stereogenic Centers on Spiropyrazolones via Organocascade Michael/Michael/1, 2-Addition Reactions. Org. Lett. 2014, 16, 2954-2957.
    • (2014) Org. Lett , vol.16 , pp. 2954-2957
    • Chauhan, P.1    Mahajan, S.2    Loh, C.C.J.3    Raabe, G.4    Enders, D.5
  • 10
    • 80052743131 scopus 로고    scopus 로고
    • Highly enantioselective cascade synthesis of spiropyrazolones
    • Zea, A.; Alba, A.N.R.; Mazzanti, A.; Moyano, A.; Rios, R. Highly enantioselective cascade synthesis of spiropyrazolones. Org. Biomol. Chem. 2011, 9, 6519-6523.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 6519-6523
    • Zea, A.1    Alba, A.N.R.2    Mazzanti, A.3    Moyano, A.4    Rios, R.5
  • 12
    • 84868031109 scopus 로고    scopus 로고
    • Enantioselective construction of multifunctionalized spirocyclohexaneoxindoles through organocatalytic Michael-Aldol cyclization of isatin derived alkenes with linear dialdehydes
    • Huang, X.; Liu, Z.; Geng, Z.; Zhang, S.; Wang, Y.; Wang, X. Enantioselective construction of multifunctionalized spirocyclohexaneoxindoles through organocatalytic Michael-Aldol cyclization of isatin derived alkenes with linear dialdehydes. Org. Biomol. Chem. 2012, 10, 8794-8799.
    • (2012) Org. Biomol. Chem , vol.10 , pp. 8794-8799
    • Huang, X.1    Liu, Z.2    Geng, Z.3    Zhang, S.4    Wang, Y.5    Wang, X.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.