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Volumn 53, Issue 14, 2012, Pages 1768-1771

Primary amine catalyzed aldol reaction of isatins and acetaldehyde

Author keywords

Acetaldehyde; Aldol; Enantioselective; Isatin; Quinine amine

Indexed keywords

ACETALDEHYDE; ALDEHYDE; ALKALOID; AMINE; ISATIN DERIVATIVE; KETONE; QUININE;

EID: 84862793386     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.01.108     Document Type: Article
Times cited : (68)

References (95)
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    • For reports of the enantioselective addition of acetaldehyde to isatin by using organocatalysts, see
    • For reports of the enantioselective addition of acetaldehyde to isatin by using organocatalysts, see: N. Hara, S. Nakamura, N. Shibata, and T. Toru Chem. Eur. J. 15 2009 6790 6793
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  • 52
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    • For examples of using activated carbonyl compounds in organocatalyzed aldol reactions, see
    • For examples of using activated carbonyl compounds in organocatalyzed aldol reactions, see: Z. Shen, B. Li, L. Wang, and Y. Zhang Tetrahedron Lett. 46 2005 8785 8788
    • (2005) Tetrahedron Lett. , vol.46 , pp. 8785-8788
    • Shen, Z.1    Li, B.2    Wang, L.3    Zhang, Y.4
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    • For selected examples of primary amine catalyzed enantioselective reactions, see
    • For selected examples of primary amine catalyzed enantioselective reactions, see: C.M. Reisinger, X. Wang, and B. List Angew. Chem., Int. Ed. 47 2008 8112 8115
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 8112-8115
    • Reisinger, C.M.1    Wang, X.2    List, B.3
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    • for a review on primary amine catalysis, see
    • for a review on primary amine catalysis, see: F. Peng, and Z.J. Shao Mol. Catal. A 285 2008 1 13
    • (2008) Mol. Catal. A , vol.285 , pp. 1-13
    • Peng, F.1    Shao, Z.J.2
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    • During the progress of our research, Cheng and coworkers published a chiral primary-tertiary diamine catalyzed aldol reaction of acetaldehyde and isatins, see
    • During the progress of our research, Cheng and coworkers published a chiral primary-tertiary diamine catalyzed aldol reaction of acetaldehyde and isatins, see: S.-S. Hu, L. Zhang, J.-Y. Li, S.-Z. Luo, and J.-P. Cheng Eur. J. Org Chem. 2011 3347 3352
    • (2011) Eur. J. Org Chem. , pp. 3347-3352
    • Hu, S.-S.1    Zhang, L.2    Li, J.-Y.3    Luo, S.-Z.4    Cheng, J.-P.5
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    • For selected examples, see: J.G. Hernandez, and E. Juaristi Tetrahedron 67 2011 6953 6959
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    • The relative stereochemistry of the two stereogenic centers in this compound was determined by reducing product 21 to the corresponding diol, for which the stereochemistry is known. For details, please see the Supplementary data and
    • The relative stereochemistry of the two stereogenic centers in this compound was determined by reducing product 21 to the corresponding diol, for which the stereochemistry is known. For details, please see the Supplementary data and: Higuchi, K.; Saito, K.; Hirayama, T.; Watanabe, Y.; Kobayashi, E.; Kawasaki, T. Synthesis 2010, 3609-3614.
    • (2010) Synthesis , pp. 3609-3614
    • Higuchi, K.1    Saito, K.2    Hirayama, T.3    Watanabe, Y.4    Kobayashi, E.5    Kawasaki, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.