An Improved Reduction of the Ester Moiety in N-Substituted Pyroglutamates-Reference-Cited by-同舟云学术

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An Improved Reduction of the Ester Moiety in N-Substituted Pyroglutamates

Published:1989-09 Issue:16 Volume:19 Page:2859-2868
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Keusenkothen Paul F.,Smith Michael B.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397918908052674

Reference11 articles.

1. Syntheses of (S)-5-substituted 4-aminopentanoic acids: a new class of .gamma.-aminobutyric acid transaminase inactivators

2. Inhibitors of GABA metabolism

3. Palfreyman , M. G. Huot , S. Lippert , B. and Schechter , P. J. 1979. Gaba-Neurotransmitters, Edited by: Krogsgaard-Larsen , P. 432–446. Copenhagen: Munksgaard.

4. Lithium aluminum hydride on silica gel - selective reduction of ketones and carboxy esters in the presence of nitro and cyano groups

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3. Tetrabutylammonium Iodide;Encyclopedia of Reagents for Organic Synthesis;2008-09-15

4. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22

5. Tetra-n-butylammonium Iodide;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

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