Synthesis of Chiral Tetrahydro-3-benzazepine Motifs by Iridium-Catalyzed Asymmetric Hydrogenation of Cyclic Ene-carbamates-Reference-Cited by-同舟云学术

Synthesis of Chiral Tetrahydro-3-benzazepine Motifs by Iridium-Catalyzed Asymmetric Hydrogenation of Cyclic Ene-carbamates

Published:2022-03-03 Issue:10 Volume:24 Page:1969-1973
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Peters Bram B. C.¹^ORCID,Andersson Pher G.¹²^ORCID,Ruchirawat Somsak³⁴⁵,Ieawsuwan Winai³⁴^ORCID

Affiliation:

1. Department of Organic Chemistry, Stockholm University, Svante Arrhenius väg 16C, SE-10691 Stockholm, Sweden

2. School of Chemistry and Physics, University of KwaZulu-Natal, Private Bag X54001, Durban 4000, South Africa

3. Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6 Road, Bangkok 10210, Thailand

4. Center of Excellence on Environmental Health and Toxicology (EHT), Office of the Permanent Secretary (OPS), Ministry of Higher Education, Science, Research and Innovation (MHESI), Bangkok 10400, Thailand

5. Program in Chemical Sciences, Chulabhorn Graduate Institute, Chulabhorn Royal Academy, 906 Kamphaeng Phet 6 Road, Bangkok 10210, Thailand

Funder

Chulabhorn Research Institute

Thailand Science Research and Innovation

Vetenskapsr?det

Knut och Alice Wallenbergs Stiftelse

Stiftelsen Olle Engkvist Byggm?stare

Development and Promotion of Science and Technology Talents Project

Center of Excellence on Environmental Health and Toxicology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00362

Reference47 articles.

1. Recent Progress in Development of Dopamine Receptor Subtype-Selective Agents: Potential Therapeutics for Neurological and Psychiatric Disorders

2. Dopamine D1receptor ligands: Where are we now and where are we going

3. Hydrogenated benzazepines: recent advances in the synthesis and study of biological activity

4. Synthesis and dopaminergic binding of 2-aryldopamine analogs: phenethylamines, 3-benzazepines, and 9-(aminomethyl)fluorenes

5. Synthesis and renal vasodilator activity of some dopamine agonist 1-aryl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diols: halogen and methyl analogs of fenoldopam

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