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Molecules 1998, 3(3), 60-63; doi:10.3390/30300060
Article

Intramolecular Cycloaddition of Imines of Cysteine Derivatives

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Received: 3 December 1997; Accepted: 3 February 1998 / Published: 18 February 1998
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Abstract: Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield.
Keywords: Thieno[3; 4-b]pyrrole derivatives; synthesis Thieno[3; 4-b]pyrrole derivatives; synthesis
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MDPI and ACS Style

Cabral, A.M.T.D.P.V.; D'A Rocha Gonsalves, A.M.; Pinho e Melo, T.M.V.D. Intramolecular Cycloaddition of Imines of Cysteine Derivatives. Molecules 1998, 3, 60-63.

AMA Style

Cabral AMTDPV, D'A Rocha Gonsalves AM, Pinho e Melo TMVD. Intramolecular Cycloaddition of Imines of Cysteine Derivatives. Molecules. 1998; 3(3):60-63.

Chicago/Turabian Style

Cabral, Ana M. T. D. P. V.; D'A Rocha Gonsalves, António M.; Pinho e Melo, Teresa M.V.D. 1998. "Intramolecular Cycloaddition of Imines of Cysteine Derivatives." Molecules 3, no. 3: 60-63.



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