Diastereoselective Synthesis of Substituted Tetrahydroquinoline-4-carboxylic Esters by a Tandem Reduction−Reductive Amination Reaction-Reference-Cited by-同舟云学术

Diastereoselective Synthesis of Substituted Tetrahydroquinoline-4-carboxylic Esters by a Tandem Reduction−Reductive Amination Reaction

Published:2001-03-16 Issue:8 Volume:66 Page:2822-2827
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bunce Richard A.¹,Herron Derrick M.¹,Johnson Lara B.¹,Kotturi Sharadsrikar V.¹

Affiliation:

1. Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma 74078-3071

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001761n

Reference22 articles.

1. Undergraduate research participant, 1999−2001.

2. Aryl-Fused Nitrogen Heterocycles by a Tandem Reduction−Michael Addition Reaction

3. Commercially available 2-nitrophenylacetic acid was esterified using MeOH/HCl (g); see: Furniss, B. S.; Hannaford, A. J.; Smith, P. W. G.; Tatchell, A. R.Vogel's Textbook of Practical Organic Chemistry, 5th ed.; Longman: New York, 1989; p 700.

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