Journal article 266 views
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization
Fei Zhao,
Domiziana Masci,
Salvatore Ferla
,
Carmine Varricchio,
Andrea Brancale,
Serena Colonna,
Gary W. Black,
Nicholas J. Turner,
Daniele Castagnolo
ACS Catalysis, Volume: 10, Issue: 11, Pages: 6414 - 6421
Swansea University Author:
Salvatore Ferla
Full text not available from this repository: check for access using links below.
DOI (Published version): 10.1021/acscatal.0c01351
Abstract
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization
Published in: | ACS Catalysis |
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ISSN: | 2155-5435 2155-5435 |
Published: |
American Chemical Society (ACS)
2020
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URI: | https://cronfa.swan.ac.uk/Record/cronfa55225 |
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2020-11-05T13:33:35.9432779 v2 55225 2020-09-20 Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization d4c62248f510e3b221916989a7bbe6a6 0000-0002-5918-9237 Salvatore Ferla Salvatore Ferla true false 2020-09-20 PHAR Journal Article ACS Catalysis 10 11 6414 6421 American Chemical Society (ACS) 2155-5435 2155-5435 5 6 2020 2020-06-05 10.1021/acscatal.0c01351 http://orca.cf.ac.uk/133403/ COLLEGE NANME Pharmacy COLLEGE CODE PHAR Swansea University 2020-11-05T13:33:35.9432779 2020-09-20T14:04:00.1831210 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Fei Zhao 1 Domiziana Masci 2 Salvatore Ferla 0000-0002-5918-9237 3 Carmine Varricchio 4 Andrea Brancale 5 Serena Colonna 6 Gary W. Black 7 Nicholas J. Turner 8 Daniele Castagnolo 9 |
title |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization |
spellingShingle |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization Salvatore Ferla |
title_short |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization |
title_full |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization |
title_fullStr |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization |
title_full_unstemmed |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization |
title_sort |
Monoamine Oxidase (MAO-N) Biocatalyzed Synthesis of Indoles from Indolines Prepared via Photocatalytic Cyclization/Arylative Dearomatization |
author_id_str_mv |
d4c62248f510e3b221916989a7bbe6a6 |
author_id_fullname_str_mv |
d4c62248f510e3b221916989a7bbe6a6_***_Salvatore Ferla |
author |
Salvatore Ferla |
author2 |
Fei Zhao Domiziana Masci Salvatore Ferla Carmine Varricchio Andrea Brancale Serena Colonna Gary W. Black Nicholas J. Turner Daniele Castagnolo |
format |
Journal article |
container_title |
ACS Catalysis |
container_volume |
10 |
container_issue |
11 |
container_start_page |
6414 |
publishDate |
2020 |
institution |
Swansea University |
issn |
2155-5435 2155-5435 |
doi_str_mv |
10.1021/acscatal.0c01351 |
publisher |
American Chemical Society (ACS) |
college_str |
Faculty of Medicine, Health and Life Sciences |
hierarchytype |
|
hierarchy_top_id |
facultyofmedicinehealthandlifesciences |
hierarchy_top_title |
Faculty of Medicine, Health and Life Sciences |
hierarchy_parent_id |
facultyofmedicinehealthandlifesciences |
hierarchy_parent_title |
Faculty of Medicine, Health and Life Sciences |
department_str |
Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine |
url |
http://orca.cf.ac.uk/133403/ |
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0 |
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published_date |
2020-06-05T04:09:17Z |
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1763753651509133312 |
score |
10.95092 |