Chemoselective Strategy for the Direct Formation of Tetrahydro-2,5-methanobenzo[c]azepines or Azetotetrahydroisoquinolines via Regio- and Stereoselective Reactions-Reference-Cited by-同舟云学术

Chemoselective Strategy for the Direct Formation of Tetrahydro-2,5-methanobenzo[c]azepines or Azetotetrahydroisoquinolines via Regio- and Stereoselective Reactions

Published:2019-05-14 Issue:11 Volume:84 Page:7100-7112
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kovács Ervin¹²^ORCID,Huszka Balázs¹,Gáti Tamás³,Nyerges Miklós³,Faigl Ferenc¹,Mucsi Zoltán⁴

Affiliation:

1. Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest H-1111 Hungary

2. Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest H-1117 Hungary

3. Servier Research Institute of Medicinal Chemistry, Budapest H-1031 Hungary

4. Femtonics, Ltd, Budapest H-1094 Hungary

Funder

Orsz?gos Tudom?nyos Kutat?si Alapprogramok

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00798

Reference61 articles.

1. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics

2. β-Phenylethylamines and the isoquinoline alkaloids

3. Recent progress in the total synthesis of naphthyridinomycin and lemonomycin tetrahydroisoquinoline antitumor antibiotics (TAAs)

4. SYNTHESIS OF 8-AZA-D-HOMO-18-NORESTRONE METHYL ETHER

5. Tetrahydroisoquinolines. I. Preparation and analgetic activity of some 1-[2-(phenylthio)ethyl]tetrahydroisoquinolines and 1-(2-phenoxyethyl)tetrahydroisoquinolines

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