(±)-2-alkyl-1,2,3,4-tetrahydroquinoline-3-carboxylic esters by a catalyst and pressure dependent tandem reduction-reductive amination reaction

Author:

Bunce Richard A.,Nago Takahiro,Sonobe Nathan

Publisher

Wiley

Subject

Organic Chemistry

Reference21 articles.

1. a Others have also used reductive amination under hydrogenation conditions to prepare heterocyclic ring systems, see: Stevens, R. V.; Lee, A. W. M. J. Chem. Soc., Chem. Commun. 1982, 102 and 103.

2. b Kawaguchi, M.; Ohashi, J.; Kawakami, Y.; Yamamoto, Y.; Oda, J. Synthesis 1985, 701.

3. A convenient synthesis of 3,6-disubstituted 3,6-diazabicyclo[3.2.2]nonanes and 3,6-diazabicyclo[3.2.1]octanes

4. Iterative Reductive Alkylation Approach to Alkaloids: A Synthesis of (.+-.)-Monomorine I and Its C-3 Epimer

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