Iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines
We report herein a novel and efficient method for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C-P bond formation reaction features the employment of a sustainable and cost-effective iron...
Ausführliche Beschreibung
Autor*in: |
Cai, Junjie [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
2017 |
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Rechteinformationen: |
Nutzungsrecht: © 2017 Taylor & Francis Group, LLC 2017 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Phosphorus, sulfur and silicon and the related elements - Philadelphia, Pa [u.a.] : Taylor & Francis, 1989, 192(2017), 9, Seite 1068 |
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Übergeordnetes Werk: |
volume:192 ; year:2017 ; number:9 ; pages:1068 |
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DOI / URN: |
10.1080/10426507.2017.1330827 |
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10.1080/10426507.2017.1330827 doi PQ20171125 (DE-627)OLC199685187X (DE-599)GBVOLC199685187X (PRQ)i849-6ce7fb28da73aedfc9fbc969b3bc21863d249085b4cbd4340287b04684428dc10 (KEY)0015125420170000192000901068ironcatalyzedaerobicoxidativephosphonationofnarylt DE-627 ger DE-627 rakwb eng 660 540 DE-600 Cai, Junjie verfasserin aut Iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier We report herein a novel and efficient method for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C-P bond formation reaction features the employment of a sustainable and cost-effective iron salt [Fe(NO 3 ) 3 ·9H 2 O] as catalyst, the utilization of air as environmental-benign oxidant, as well as the user-friendly open-flask reaction conditions. Nutzungsrecht: © 2017 Taylor & Francis Group, LLC 2017 coupling α-aminophosphonate iron catalysis Oxidative phosphonation Synthesis (chemistry) Aromatic compounds Catalysts Iron Liu, Yingle oth Jiang, Yan oth Yang, Yi oth Enthalten in Phosphorus, sulfur and silicon and the related elements Philadelphia, Pa [u.a.] : Taylor & Francis, 1989 192(2017), 9, Seite 1068 (DE-627)130784885 (DE-600)1004997-6 (DE-576)017720621 1042-6507 nnns volume:192 year:2017 number:9 pages:1068 http://dx.doi.org/10.1080/10426507.2017.1330827 Volltext http://www.tandfonline.com/doi/abs/10.1080/10426507.2017.1330827 https://search.proquest.com/docview/1933994849 GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_4305 AR 192 2017 9 1068 |
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10.1080/10426507.2017.1330827 doi PQ20171125 (DE-627)OLC199685187X (DE-599)GBVOLC199685187X (PRQ)i849-6ce7fb28da73aedfc9fbc969b3bc21863d249085b4cbd4340287b04684428dc10 (KEY)0015125420170000192000901068ironcatalyzedaerobicoxidativephosphonationofnarylt DE-627 ger DE-627 rakwb eng 660 540 DE-600 Cai, Junjie verfasserin aut Iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier We report herein a novel and efficient method for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C-P bond formation reaction features the employment of a sustainable and cost-effective iron salt [Fe(NO 3 ) 3 ·9H 2 O] as catalyst, the utilization of air as environmental-benign oxidant, as well as the user-friendly open-flask reaction conditions. Nutzungsrecht: © 2017 Taylor & Francis Group, LLC 2017 coupling α-aminophosphonate iron catalysis Oxidative phosphonation Synthesis (chemistry) Aromatic compounds Catalysts Iron Liu, Yingle oth Jiang, Yan oth Yang, Yi oth Enthalten in Phosphorus, sulfur and silicon and the related elements Philadelphia, Pa [u.a.] : Taylor & Francis, 1989 192(2017), 9, Seite 1068 (DE-627)130784885 (DE-600)1004997-6 (DE-576)017720621 1042-6507 nnns volume:192 year:2017 number:9 pages:1068 http://dx.doi.org/10.1080/10426507.2017.1330827 Volltext http://www.tandfonline.com/doi/abs/10.1080/10426507.2017.1330827 https://search.proquest.com/docview/1933994849 GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_4305 AR 192 2017 9 1068 |
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Iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines |
abstract |
We report herein a novel and efficient method for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C-P bond formation reaction features the employment of a sustainable and cost-effective iron salt [Fe(NO 3 ) 3 ·9H 2 O] as catalyst, the utilization of air as environmental-benign oxidant, as well as the user-friendly open-flask reaction conditions. |
abstractGer |
We report herein a novel and efficient method for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C-P bond formation reaction features the employment of a sustainable and cost-effective iron salt [Fe(NO 3 ) 3 ·9H 2 O] as catalyst, the utilization of air as environmental-benign oxidant, as well as the user-friendly open-flask reaction conditions. |
abstract_unstemmed |
We report herein a novel and efficient method for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C-P bond formation reaction features the employment of a sustainable and cost-effective iron salt [Fe(NO 3 ) 3 ·9H 2 O] as catalyst, the utilization of air as environmental-benign oxidant, as well as the user-friendly open-flask reaction conditions. |
collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_4305 |
container_issue |
9 |
title_short |
Iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines |
url |
http://dx.doi.org/10.1080/10426507.2017.1330827 http://www.tandfonline.com/doi/abs/10.1080/10426507.2017.1330827 https://search.proquest.com/docview/1933994849 |
remote_bool |
false |
author2 |
Liu, Yingle Jiang, Yan Yang, Yi |
author2Str |
Liu, Yingle Jiang, Yan Yang, Yi |
ppnlink |
130784885 |
mediatype_str_mv |
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false |
hochschulschrift_bool |
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author2_role |
oth oth oth |
doi_str |
10.1080/10426507.2017.1330827 |
up_date |
2024-07-04T01:32:55.803Z |
_version_ |
1803610253756989440 |
fullrecord_marcxml |
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