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Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons
Utilization of Freon-type methanes as functional one-carbon synthons in the synthesis of various deuterated indoline alkaloids was demonstrated here. A series of halomethyl radicals were generated from electro-reductive C-X cleavage of Freon-type methanes and captured efficiently by acrylamides to p...
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Published in: | Chemical communications (Cambridge, England) England), 2022-08, Vol.58 (66), p.923-9233 |
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container_issue | 66 |
container_start_page | 923 |
container_title | Chemical communications (Cambridge, England) |
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creator | Chen, Chao Liu, Ru-Xin Xiong, Feng Li, Zi-Hao Kang, Jun-Chen Ding, Tong-Mei Zhang, Shu-Yu |
description | Utilization of Freon-type methanes as functional one-carbon synthons in the synthesis of various deuterated indoline alkaloids was demonstrated here. A series of halomethyl radicals were generated from electro-reductive C-X cleavage of Freon-type methanes and captured efficiently by acrylamides to provide various halogenated oxindoles
via
radical cyclization. This reaction features good functional group tolerance, and deuterium and fluorine atoms could be introduced facilely from Freon-type methanes. Further transformation of halogenated oxindoles enabled the synthesis of many (labeled) bioactive drug molecules and skeletons, such as deuterated (±)-physostigmine, deuterated (±)-esermethole and deuterated (±)-lansai B.
Electrochemical radical cyclization of acrylamides with Freon-type methanes as functional C1 synthons provided various halogenated oxindoles, which could be transformed into various labeled pyrroloindoline alkaloids. |
doi_str_mv | 10.1039/d2cc03301a |
format | article |
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via
radical cyclization. This reaction features good functional group tolerance, and deuterium and fluorine atoms could be introduced facilely from Freon-type methanes. Further transformation of halogenated oxindoles enabled the synthesis of many (labeled) bioactive drug molecules and skeletons, such as deuterated (±)-physostigmine, deuterated (±)-esermethole and deuterated (±)-lansai B.
Electrochemical radical cyclization of acrylamides with Freon-type methanes as functional C1 synthons provided various halogenated oxindoles, which could be transformed into various labeled pyrroloindoline alkaloids.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d2cc03301a</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Alkaloids ; Chemical synthesis ; Deuteration ; Deuterium ; Fluorine ; Freons ; Functional groups ; Physostigmine</subject><ispartof>Chemical communications (Cambridge, England), 2022-08, Vol.58 (66), p.923-9233</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-e1b70dc1f78b23c29abc842da85e8a4321dd434d2ff5efc2f804be61ba937b713</citedby><cites>FETCH-LOGICAL-c314t-e1b70dc1f78b23c29abc842da85e8a4321dd434d2ff5efc2f804be61ba937b713</cites><orcidid>0000-0002-1811-4159</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Chen, Chao</creatorcontrib><creatorcontrib>Liu, Ru-Xin</creatorcontrib><creatorcontrib>Xiong, Feng</creatorcontrib><creatorcontrib>Li, Zi-Hao</creatorcontrib><creatorcontrib>Kang, Jun-Chen</creatorcontrib><creatorcontrib>Ding, Tong-Mei</creatorcontrib><creatorcontrib>Zhang, Shu-Yu</creatorcontrib><title>Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons</title><title>Chemical communications (Cambridge, England)</title><description>Utilization of Freon-type methanes as functional one-carbon synthons in the synthesis of various deuterated indoline alkaloids was demonstrated here. A series of halomethyl radicals were generated from electro-reductive C-X cleavage of Freon-type methanes and captured efficiently by acrylamides to provide various halogenated oxindoles
via
radical cyclization. This reaction features good functional group tolerance, and deuterium and fluorine atoms could be introduced facilely from Freon-type methanes. Further transformation of halogenated oxindoles enabled the synthesis of many (labeled) bioactive drug molecules and skeletons, such as deuterated (±)-physostigmine, deuterated (±)-esermethole and deuterated (±)-lansai B.
Electrochemical radical cyclization of acrylamides with Freon-type methanes as functional C1 synthons provided various halogenated oxindoles, which could be transformed into various labeled pyrroloindoline alkaloids.</description><subject>Alkaloids</subject><subject>Chemical synthesis</subject><subject>Deuteration</subject><subject>Deuterium</subject><subject>Fluorine</subject><subject>Freons</subject><subject>Functional groups</subject><subject>Physostigmine</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkUtLAzEUhQdRsFY37oWAGxFG85rXUsZWhYIbBXdDJrlhpqZJTabKgD_e1IqCd3MffJxz4STJKcFXBLPqWlEpMWOYiL1kQljO04yXL_vbOavSgvHsMDkKYYljkaycJJ8zA3LwTnaw6qUwSDqzvfTvgMJohw5CH5DTyIgWDCi0Hr13xvVWOdNbQMK8iriqgD76oUNzD86mw7gGtIKhExYCEgHpjY2azkaDmuyEnQ3HyYEWJsDJT58mz_PZU32fLh7vHuqbRSoZ4UMKpC2wkkQXZUuZpJVoZcmpEmUGpeCMEqU444pqnYGWVJeYt5CTVlSsaAvCpsnFTnft3dsGwtCs-iDBmPie24SG5lWOCakojej5P3TpNj7-HakC02jDMxypyx0lvQvBg27Wvl8JPzYEN9sgmlta199B3ET4bAf7IH-5v6DYF1Y0h5k</recordid><startdate>20220816</startdate><enddate>20220816</enddate><creator>Chen, Chao</creator><creator>Liu, Ru-Xin</creator><creator>Xiong, Feng</creator><creator>Li, Zi-Hao</creator><creator>Kang, Jun-Chen</creator><creator>Ding, Tong-Mei</creator><creator>Zhang, Shu-Yu</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1811-4159</orcidid></search><sort><creationdate>20220816</creationdate><title>Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons</title><author>Chen, Chao ; Liu, Ru-Xin ; Xiong, Feng ; Li, Zi-Hao ; Kang, Jun-Chen ; Ding, Tong-Mei ; Zhang, Shu-Yu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-e1b70dc1f78b23c29abc842da85e8a4321dd434d2ff5efc2f804be61ba937b713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alkaloids</topic><topic>Chemical synthesis</topic><topic>Deuteration</topic><topic>Deuterium</topic><topic>Fluorine</topic><topic>Freons</topic><topic>Functional groups</topic><topic>Physostigmine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Chao</creatorcontrib><creatorcontrib>Liu, Ru-Xin</creatorcontrib><creatorcontrib>Xiong, Feng</creatorcontrib><creatorcontrib>Li, Zi-Hao</creatorcontrib><creatorcontrib>Kang, Jun-Chen</creatorcontrib><creatorcontrib>Ding, Tong-Mei</creatorcontrib><creatorcontrib>Zhang, Shu-Yu</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Chao</au><au>Liu, Ru-Xin</au><au>Xiong, Feng</au><au>Li, Zi-Hao</au><au>Kang, Jun-Chen</au><au>Ding, Tong-Mei</au><au>Zhang, Shu-Yu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><date>2022-08-16</date><risdate>2022</risdate><volume>58</volume><issue>66</issue><spage>923</spage><epage>9233</epage><pages>923-9233</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Utilization of Freon-type methanes as functional one-carbon synthons in the synthesis of various deuterated indoline alkaloids was demonstrated here. A series of halomethyl radicals were generated from electro-reductive C-X cleavage of Freon-type methanes and captured efficiently by acrylamides to provide various halogenated oxindoles
via
radical cyclization. This reaction features good functional group tolerance, and deuterium and fluorine atoms could be introduced facilely from Freon-type methanes. Further transformation of halogenated oxindoles enabled the synthesis of many (labeled) bioactive drug molecules and skeletons, such as deuterated (±)-physostigmine, deuterated (±)-esermethole and deuterated (±)-lansai B.
Electrochemical radical cyclization of acrylamides with Freon-type methanes as functional C1 synthons provided various halogenated oxindoles, which could be transformed into various labeled pyrroloindoline alkaloids.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2cc03301a</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-1811-4159</orcidid></addata></record> |
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source | Royal Society of Chemistry Journals |
subjects | Alkaloids Chemical synthesis Deuteration Deuterium Fluorine Freons Functional groups Physostigmine |
title | Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons |
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