Lista de obras - Richard L. Apodaca - Dominio Público Uruguay

1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase

artículo científico publicado en 2014

4-phenoxypiperidines: potent, conformationally restricted, non-imidazole histamine H3 antagonists

artículo científico publicado en 2005

A convenient synthesis of protected and free homoallylic alcohols: Catalytic use of dibutyltin dichloride in the allylation of aldehydes with allyltributyltin

A new class of diamine-based human histamine H3 receptor antagonists: 4-(aminoalkoxy)benzylamines

artículo científico publicado en 2003

Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist

artículo científico publicado en 2004

Aplysamine-1 and related analogs as histamine H3 receptor antagonists

artículo científico publicado en 2005

Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate

artículo científico publicado en 2012

Biochemical and biological properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a mechanism-based inhibitor of fatty acid amide hydrolase

artículo científico publicado en 2009

Comphrehensive Organic Functional Group Transformations, Volumes 1−7 Edited by Alan R. Katritzky, Otto Meth-Cohn, and Charles W. Rees. Elsevier: Amsterdam. 1996. 7500+ pp. $6846.00. ISBN 0-08-040604-1

article

Corrigendum to acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist.

artículo científico publicado en 2005

Diamine-based human histamine H3 receptor antagonists: (4-aminobutyn-1-yl)benzylamines

artículo científico publicado en 2009

Direct Reductive Amination of Aldehydes and Ketones Using Phenylsilane: Catalysis by Dibutyltin Dichloride

artículo científico publicado en 2001

Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists

artículo científico publicado en 2009

Lead identification of acetylcholinesterase inhibitors-histamine H3 receptor antagonists from molecular modeling

artículo científico publicado en 2007

Mobile apps for chemistry in the world of drug discovery

artículo científico

Novel benzamide-based histamine h3 receptor antagonists: the identification of two candidates for clinical development

artículo científico publicado en 2015

Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH).

artículo científico publicado en 2008

Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase

artículo científico publicado en 2007

Studies in enantioselective catalysis : (1) a new class of chiral C₂-symmetric bisphenols ; (2) Diorganotin

PhD thesis from 1996

Synthesis and resolution of a new chiral C2-symmetric bisphenol: trans-1,2-bis(2-hydroxyphenyl)cyclopentane

The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitors

artículo científico publicado en 2016

Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase

artículo científico publicado en 2008

Lista de obras de Richard L. Apodaca

1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase

4-phenoxypiperidines: potent, conformationally restricted, non-imidazole histamine H3 antagonists

A convenient synthesis of protected and free homoallylic alcohols: Catalytic use of dibutyltin dichloride in the allylation of aldehydes with allyltributyltin

A new class of diamine-based human histamine H3 receptor antagonists: 4-(aminoalkoxy)benzylamines

Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist

Aplysamine-1 and related analogs as histamine H3 receptor antagonists

Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate

Biochemical and biological properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a mechanism-based inhibitor of fatty acid amide hydrolase

Comphrehensive Organic Functional Group Transformations, Volumes 1−7 Edited by Alan R. Katritzky, Otto Meth-Cohn, and Charles W. Rees. Elsevier: Amsterdam. 1996. 7500+ pp. $6846.00. ISBN 0-08-040604-1

Corrigendum to acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist.

Diamine-based human histamine H3 receptor antagonists: (4-aminobutyn-1-yl)benzylamines

Direct Reductive Amination of Aldehydes and Ketones Using Phenylsilane: Catalysis by Dibutyltin Dichloride

Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists

Lead identification of acetylcholinesterase inhibitors-histamine H3 receptor antagonists from molecular modeling

Mobile apps for chemistry in the world of drug discovery

Novel benzamide-based histamine h3 receptor antagonists: the identification of two candidates for clinical development

Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH).

Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase

Studies in enantioselective catalysis : (1) a new class of chiral C₂-symmetric bisphenols ; (2) Diorganotin

Synthesis and resolution of a new chiral C2-symmetric bisphenol: trans-1,2-bis(2-hydroxyphenyl)cyclopentane

The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitors

Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase

Trimethylsilylcyanation of aldehydes and ketones catalyzed by diorganotin dichlorides