Stereospecificity of Retinol Saturase: Absolute Configuration, Synthesis, and Biological Evaluation of Dihydroretinoids-Reference-Cited by-同舟云学术

Stereospecificity of Retinol Saturase: Absolute Configuration, Synthesis, and Biological Evaluation of Dihydroretinoids

Published:2008-01-08 Issue:4 Volume:130 Page:1154-1155
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Moise Alexander R.¹,Domínguez Marta¹,Alvarez Susana¹,Alvarez Rosana¹,Schupp Michael¹,Cristancho Ana G.¹,Kiser Philip D.¹,de Lera Angel R.¹,Lazar Mitchell A.¹,Palczewski Krzysztof¹

Affiliation:

1. Department of Pharmacology, Case School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4965, Departamento de Química Orgánica, Facultad de Química, Universidade de Vigo, 36310 Vigo, Spain, and Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine and Department of Genetics, and The Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja710487q

Reference10 articles.

1. Identification of All-trans-Retinol:All-trans-13,14-dihydroretinol Saturase

2. Metabolism and Transactivation Activity of 13,14-Dihydroretinoic Acid

3. Stereoselective conjugate addition of organolithium and organocopper reagents to δ-oxygenated α,β-unsaturated carbonyl systems derived from glyceraldehyde acetonide

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