Secondary compounds in the catalytic hydrogenation of enone and allylic alcohol prostaglandin intermediates: isolation, characterization, and X-ray crystallography-Reference-Cited by-同舟云学术

Secondary compounds in the catalytic hydrogenation of enone and allylic alcohol prostaglandin intermediates: isolation, characterization, and X-ray crystallography

Published:2019 Issue:20 Volume:43 Page:7582-7599
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Tănase Constantin I.¹²³^ORCID,Cocu Florea¹²³,Drăghici Constantin⁴⁵³,Hanganu Anamaria⁴⁵³^ORCID,Pintilie Lucia¹²³^ORCID,Maganu Maria⁴⁵³,Munteanu Cristian V. A.⁶⁷³^ORCID,Shova Sergiu⁸⁹³^ORCID

Affiliation:

1. National Institute for Chemical-Pharmaceutical Research and Development

2. Bucharest-3

3. Romania

4. Organic Chemistry Center “C.D.Nenitescu”

5. 060023 Bucharest

6. Romanian Academy-Institute of Biochemistry (IBAR)

7. Bucharest

8. Institute of Macromolecular Chemistry “Petru Poni”

9. 700478 Iasi

Abstract

Hydrogenation of the double bond in the ω-side chain of prostaglandin intermediates: conditions to increase the yield and minimize the formation of secondary compounds.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ01186B

Reference10 articles.

1. Phenyl-substituted prostaglandins: potent and selective antiglaucoma agents

2. Effect of Alkali Salts on the Steric Course of Hydrogenation of a Cyclic Allylic Alcohol

3. A new chemoenzymatic approach to the synthesis of Latanoprost and Bimatoprost

4. Discovery, Characterization, Engineering, and Applications of Ene-Reductases for Industrial Biocatalysis

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