A new approach to 3-substituted tetrahydro-β-carboline derivative via diethyl acetamidomalonate
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Clinical Biochemistry,Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s00726-010-0792-z.pdf
Reference25 articles.
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3. Cook JM, Cox ED (1995) The Pictet–Spengler condensation: a new direction for an old reaction. Chem Rev 95:1797–1842 (and references cited therein)
4. Cook JM, Yin W, Kabir MS, Wang Z, Rallapalli SK, Ma J (2010) Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A. J Org Chem 75:3339–3349
5. Fujii N, Ohno H, Oishi S, Ohta Y (2009) Facile synthesis of 1,2,3,4-tetrahydro-β-carbolines by one-pot domino three-component indole formation and nucleophilic cyclization. Org Lett 11:1979–1982
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