Amino Acid Catalyzed Conjugate Addition of Thiol to Dienone

Han Feng Cui; Yan Lin; Hao Fan; Li De Yu; Ping Nan Wan

doi:10.4028/www.scientific.net/AMR.834-836.450

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HomeAdvanced Materials ResearchAdvanced Materials Research Vols. 834-836Amino Acid Catalyzed Conjugate Addition of Thiol...

Amino Acid Catalyzed Conjugate Addition of Thiol to Dienone

Abstract:

Double conjugate addition of thiols with dienones was catalyzed by amino acids at room temperature in methanol, to afford the corresponding addition product in good to excellent yields.

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Periodical:

Advanced Materials Research (Volumes 834-836)

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450-453

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https://doi.org/10.4028/www.scientific.net/AMR.834-836.450

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Online since:

October 2013

Authors:

Han Feng Cui*, Yan Lin, Hao Fan, Li De Yu, Ping Nan Wan

Keywords:

Amino Acids, Conjugate Addition, Dienones, Thiols

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References

[1] A. Dondoni and A. Massi: Angew. Chem. Int. Ed. Vol. 47 (2008), p.4638.

Google Scholar

[2] S. Mukherjee, J. W. Yang, S. Hoffmann and B. List: Chem. Rev. Vol. 107 (2007), p.5471.

Google Scholar

[3] E. Emori, T. Arai, H. Sasai and M. Shibasaki: J. Am. Chem. Soc. Vol. 120 (1998), p.4043.

Google Scholar

[4] P. Laszlo, M. -T. Montaufier and S. L. Randriamahefa: Tetrahedron Lett. Vol. 31 (1990), p.4867.

Google Scholar

[5] M. Bandini, P. G. Cozzi, M. Giacomini, P. Melchiorre, S. Selva and A. Umani-Ronchi: J. Org. Chem. Vol. 67 (2002), p.3700.

DOI: 10.1021/jo0163243

Google Scholar

[6] M. M. Alam, R. Varala and S. R. Adapa: Tetrahedron Lett. Vol. 44 (2003), p.5115.

Google Scholar

[7] S. Kobayashi, C. Ogawa, M. Kawamura and M. Sugiura: Synlett Vol. 2001, p.983.

Google Scholar

[8] S. K. Garg, R. Kumar and A. K. Chakraborti: Tetrahedron Lett. Vol. 46 (2005), p.1721.

Google Scholar

[9] A. Kumar and Akanksha: Tetrahedron Vol. 63 (2007), p.11086.

Google Scholar

[10] C. -M. Chu, S Gao, M. N. V. Sastry and C. -F. Yao: Tetrahedron Lett. Vol. 46 (2005), p.4971.

Google Scholar

[11] W. Y. Chen and L. Shi: Catal. Commun. Vol. 9 (2008), p.1079.

Google Scholar

[12] F. M. Moghaddam, G. R. Bardajee, and R. O. C. Veranlou: Synthetic Commun. Vol. 35 (2005), p.2427.

Google Scholar

[13] L. D. Yu, H. F. Cui, H. Fan, S. H. Ren and Y. Lin: Progress in Chemistry. Vol. 25 (2013), p.744 (In Chinese).

Google Scholar