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Domino Oxidative Cyclization of 2-Aminoacetophenones for the One-Pot Synthesis of Tryptanthrin Derivatives
A new CuI/DMSO‐mediated oxidative domino process has been developed for the synthesis of tryptanthrin derivatives. This is the first example of the synthesis of tryptanthrin derivatives directly from 2‐aminoaryl methyl ketones and isatoic anhydrides through copper‐promoted oxidative functionalizatio...
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Published in: | European journal of organic chemistry 2015-12, Vol.2015 (36), p.8018-8022 |
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cited_by | cdi_FETCH-LOGICAL-c2009-b0d74daceaae1228ba7c37f4edb3c8c7c45542c67af5959e72db41706d848af3 |
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cites | cdi_FETCH-LOGICAL-c2009-b0d74daceaae1228ba7c37f4edb3c8c7c45542c67af5959e72db41706d848af3 |
container_end_page | 8022 |
container_issue | 36 |
container_start_page | 8018 |
container_title | European journal of organic chemistry |
container_volume | 2015 |
creator | Reddy, B. V. Subba Reddy, D. Maheswara Reddy, G. Niranjan Reddy, M. Ramana Reddy, V. Krishna |
description | A new CuI/DMSO‐mediated oxidative domino process has been developed for the synthesis of tryptanthrin derivatives. This is the first example of the synthesis of tryptanthrin derivatives directly from 2‐aminoaryl methyl ketones and isatoic anhydrides through copper‐promoted oxidative functionalization.
A new DMSO/CuI‐catalysed oxidative domino process has been developed for the one‐pot synthesis of tryptanthrin derivatives. |
doi_str_mv | 10.1002/ejoc.201501079 |
format | article |
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A new DMSO/CuI‐catalysed oxidative domino process has been developed for the one‐pot synthesis of tryptanthrin derivatives.</description><subject>1-b]quinazolines</subject><subject>2-Aminoacetophenone</subject><subject>Indolo</subject><subject>Indolo[2,1‐b]quinazolines</subject><subject>Isatoic anhydride</subject><subject>Nitrogen heterocycles</subject><subject>Synthetic methods</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkM1OAjEUhSdGExHdum7ievB2pjOdLhEUf4gYJJFdUzqdUIQptgMyvpMv4ZNZxBB3ru5PznfPzQmCcwwtDBBdqpmRrQhwAhgoOwgaGBgLIWVw6HsSkxCzeHwcnDg3AwCWprgRzLtmoUuDBhudi0qvFerUcq4_fG9KZAoUhe2t4OtTSFWZ5VSVplQOFcaiaqrQoFThk6nQc1360Wm3ZUa2XlbCL6wuUVdZvf457U6Do0LMnTr7rc1gdHM96tyG_UHvrtPuhzLyf4UTyCnJvZ8QCkdRNhFUxrQgKp_EMpNUkiQhkUypKBKWMEWjfEIwhTTPSCaKuBlc7M4urXlbKVfxmVnZ0jtyTEkGCZCUeVVrp5LWOGdVwZdWL4StOQa-DZRvA-X7QD3AdsC7nqv6HzW_vh90_rLhjtWuUps9K-wrT2lME_7y2OPjIek_DIdXPI2_AUimjC0</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Reddy, B. V. Subba</creator><creator>Reddy, D. Maheswara</creator><creator>Reddy, G. Niranjan</creator><creator>Reddy, M. Ramana</creator><creator>Reddy, V. Krishna</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201512</creationdate><title>Domino Oxidative Cyclization of 2-Aminoacetophenones for the One-Pot Synthesis of Tryptanthrin Derivatives</title><author>Reddy, B. V. Subba ; Reddy, D. Maheswara ; Reddy, G. Niranjan ; Reddy, M. Ramana ; Reddy, V. Krishna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2009-b0d74daceaae1228ba7c37f4edb3c8c7c45542c67af5959e72db41706d848af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>1-b]quinazolines</topic><topic>2-Aminoacetophenone</topic><topic>Indolo</topic><topic>Indolo[2,1‐b]quinazolines</topic><topic>Isatoic anhydride</topic><topic>Nitrogen heterocycles</topic><topic>Synthetic methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reddy, B. V. Subba</creatorcontrib><creatorcontrib>Reddy, D. Maheswara</creatorcontrib><creatorcontrib>Reddy, G. Niranjan</creatorcontrib><creatorcontrib>Reddy, M. Ramana</creatorcontrib><creatorcontrib>Reddy, V. Krishna</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reddy, B. V. Subba</au><au>Reddy, D. Maheswara</au><au>Reddy, G. Niranjan</au><au>Reddy, M. Ramana</au><au>Reddy, V. Krishna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Domino Oxidative Cyclization of 2-Aminoacetophenones for the One-Pot Synthesis of Tryptanthrin Derivatives</atitle><jtitle>European journal of organic chemistry</jtitle><addtitle>Eur. J. Org. Chem</addtitle><date>2015-12</date><risdate>2015</risdate><volume>2015</volume><issue>36</issue><spage>8018</spage><epage>8022</epage><pages>8018-8022</pages><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>A new CuI/DMSO‐mediated oxidative domino process has been developed for the synthesis of tryptanthrin derivatives. This is the first example of the synthesis of tryptanthrin derivatives directly from 2‐aminoaryl methyl ketones and isatoic anhydrides through copper‐promoted oxidative functionalization.
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subjects | 1-b]quinazolines 2-Aminoacetophenone Indolo Indolo[2,1‐b]quinazolines Isatoic anhydride Nitrogen heterocycles Synthetic methods |
title | Domino Oxidative Cyclization of 2-Aminoacetophenones for the One-Pot Synthesis of Tryptanthrin Derivatives |
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