Loading…
Synthesis of tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation
We report a palladium‐catalyzed intramolecular direct heteroarylation of oxazole tethered β ‐naphthols to access corresponding tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles. Various functional groups are well tolerated and furnished the desired products in good to excellent yields under the p...
Saved in:
Published in: | Chemistry, an Asian journal an Asian journal, 2023-02, Vol.18 (3) |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-crossref_primary_10_1002_asia_2022011513 |
container_end_page | |
container_issue | 3 |
container_start_page | |
container_title | Chemistry, an Asian journal |
container_volume | 18 |
creator | Kumar, Sujeet Kajol, Km Nayak, Prakash Kumar, Amit Ramesh, Chintakunta |
description | We report a palladium‐catalyzed intramolecular direct heteroarylation of oxazole tethered
β
‐naphthols to access corresponding tetracyclic 4
H
‐benzo[5,6]chromeno[3,4‐
d
]oxazoles. Various functional groups are well tolerated and furnished the desired products in good to excellent yields under the present reaction conditions. The scale‐up reaction and synthetic utility of the resulting molecules have been demonstrated. Moreover, UV/vis absorption and fluorescence emission properties have been evaluated for these polyheterocyclic compounds. |
doi_str_mv | 10.1002/asia.202201151 |
format | article |
fullrecord | <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1002_asia_202201151</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1002_asia_202201151</sourcerecordid><originalsourceid>FETCH-crossref_primary_10_1002_asia_2022011513</originalsourceid><addsrcrecordid>eNqVj81KAzEUhYMoWK1b1_cB2jFJZ-q4FqV7uxBKCbeZO0wkk5QkFWdWbtz7jD6JKUj3rs6B8wMfY7eCF4JzeYfRYCG5lFyISpyxiaiXYl7ei9fzk5f1JbuK8Y3zSvKHesK-XgaXOoomgm8hUQqoB22NhhJW8PP5vSM3-k01W251F3xPzm8WszIH0MDWf-DoLUV4Nwh7tBYbc-hzqDGhHUZqwLh82eeSPlgM0JhAOkFHiYLHMFhMxrspu2jRRrr502tWPD-tH1dzHXyMgVq1D6bPdSW4OsKqI6w6wS7-PfgF0sJihQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Kumar, Sujeet ; Kajol, Km ; Nayak, Prakash ; Kumar, Amit ; Ramesh, Chintakunta</creator><creatorcontrib>Kumar, Sujeet ; Kajol, Km ; Nayak, Prakash ; Kumar, Amit ; Ramesh, Chintakunta</creatorcontrib><description>We report a palladium‐catalyzed intramolecular direct heteroarylation of oxazole tethered
β
‐naphthols to access corresponding tetracyclic 4
H
‐benzo[5,6]chromeno[3,4‐
d
]oxazoles. Various functional groups are well tolerated and furnished the desired products in good to excellent yields under the present reaction conditions. The scale‐up reaction and synthetic utility of the resulting molecules have been demonstrated. Moreover, UV/vis absorption and fluorescence emission properties have been evaluated for these polyheterocyclic compounds.</description><identifier>ISSN: 1861-4728</identifier><identifier>EISSN: 1861-471X</identifier><identifier>DOI: 10.1002/asia.202201151</identifier><language>eng</language><ispartof>Chemistry, an Asian journal, 2023-02, Vol.18 (3)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-crossref_primary_10_1002_asia_2022011513</cites><orcidid>0000-0001-7327-4430</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kumar, Sujeet</creatorcontrib><creatorcontrib>Kajol, Km</creatorcontrib><creatorcontrib>Nayak, Prakash</creatorcontrib><creatorcontrib>Kumar, Amit</creatorcontrib><creatorcontrib>Ramesh, Chintakunta</creatorcontrib><title>Synthesis of tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation</title><title>Chemistry, an Asian journal</title><description>We report a palladium‐catalyzed intramolecular direct heteroarylation of oxazole tethered
β
‐naphthols to access corresponding tetracyclic 4
H
‐benzo[5,6]chromeno[3,4‐
d
]oxazoles. Various functional groups are well tolerated and furnished the desired products in good to excellent yields under the present reaction conditions. The scale‐up reaction and synthetic utility of the resulting molecules have been demonstrated. Moreover, UV/vis absorption and fluorescence emission properties have been evaluated for these polyheterocyclic compounds.</description><issn>1861-4728</issn><issn>1861-471X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqVj81KAzEUhYMoWK1b1_cB2jFJZ-q4FqV7uxBKCbeZO0wkk5QkFWdWbtz7jD6JKUj3rs6B8wMfY7eCF4JzeYfRYCG5lFyISpyxiaiXYl7ei9fzk5f1JbuK8Y3zSvKHesK-XgaXOoomgm8hUQqoB22NhhJW8PP5vSM3-k01W251F3xPzm8WszIH0MDWf-DoLUV4Nwh7tBYbc-hzqDGhHUZqwLh82eeSPlgM0JhAOkFHiYLHMFhMxrspu2jRRrr502tWPD-tH1dzHXyMgVq1D6bPdSW4OsKqI6w6wS7-PfgF0sJihQ</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Kumar, Sujeet</creator><creator>Kajol, Km</creator><creator>Nayak, Prakash</creator><creator>Kumar, Amit</creator><creator>Ramesh, Chintakunta</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-7327-4430</orcidid></search><sort><creationdate>202302</creationdate><title>Synthesis of tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation</title><author>Kumar, Sujeet ; Kajol, Km ; Nayak, Prakash ; Kumar, Amit ; Ramesh, Chintakunta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-crossref_primary_10_1002_asia_2022011513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Sujeet</creatorcontrib><creatorcontrib>Kajol, Km</creatorcontrib><creatorcontrib>Nayak, Prakash</creatorcontrib><creatorcontrib>Kumar, Amit</creatorcontrib><creatorcontrib>Ramesh, Chintakunta</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry, an Asian journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Sujeet</au><au>Kajol, Km</au><au>Nayak, Prakash</au><au>Kumar, Amit</au><au>Ramesh, Chintakunta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation</atitle><jtitle>Chemistry, an Asian journal</jtitle><date>2023-02</date><risdate>2023</risdate><volume>18</volume><issue>3</issue><issn>1861-4728</issn><eissn>1861-471X</eissn><abstract>We report a palladium‐catalyzed intramolecular direct heteroarylation of oxazole tethered
β
‐naphthols to access corresponding tetracyclic 4
H
‐benzo[5,6]chromeno[3,4‐
d
]oxazoles. Various functional groups are well tolerated and furnished the desired products in good to excellent yields under the present reaction conditions. The scale‐up reaction and synthetic utility of the resulting molecules have been demonstrated. Moreover, UV/vis absorption and fluorescence emission properties have been evaluated for these polyheterocyclic compounds.</abstract><doi>10.1002/asia.202201151</doi><orcidid>https://orcid.org/0000-0001-7327-4430</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1861-4728 |
ispartof | Chemistry, an Asian journal, 2023-02, Vol.18 (3) |
issn | 1861-4728 1861-471X |
language | eng |
recordid | cdi_crossref_primary_10_1002_asia_202201151 |
source | Wiley-Blackwell Read & Publish Collection |
title | Synthesis of tetracyclic 4 H ‐benzo[5,6]chromeno[3,4‐ d ]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T09%3A57%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20tetracyclic%204%20H%20%E2%80%90benzo%5B5,6%5Dchromeno%5B3,4%E2%80%90%20d%20%5Doxazoles%20via%20palladium%E2%80%90catalyzed%20intramolecular%20direct%20heteroarylation&rft.jtitle=Chemistry,%20an%20Asian%20journal&rft.au=Kumar,%20Sujeet&rft.date=2023-02&rft.volume=18&rft.issue=3&rft.issn=1861-4728&rft.eissn=1861-471X&rft_id=info:doi/10.1002/asia.202201151&rft_dat=%3Ccrossref%3E10_1002_asia_202201151%3C/crossref%3E%3Cgrp_id%3Ecdi_FETCH-crossref_primary_10_1002_asia_2022011513%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |