Loading…

Synthesis of 2-azetidinones substituted coumarin derivative

?-Naphthol is converted into 4-methylbenzo[h]chromen-2-one by reacting with ethyl acetoacetate in the presence of bismuth trichloride which is then oxidized to 2-oxo-2H-benzo[h]chromene-4-carbaldehyde and then condensed with aromatic primary amines to give Schiff bases (3a-3d). These Schiff bases ar...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the Serbian Chemical Society 2012, Vol.77 (10), p.1339-1344
Main Authors: Mashelkar, Uday, Jha, Mukesh, Mashelkar, Beena
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c187m-d7cf90d2f0d630fe7dad52180e18f0e9f56e547b9ef86e9f8ebbe790efd170f93
cites
container_end_page 1344
container_issue 10
container_start_page 1339
container_title Journal of the Serbian Chemical Society
container_volume 77
creator Mashelkar, Uday
Jha, Mukesh
Mashelkar, Beena
description ?-Naphthol is converted into 4-methylbenzo[h]chromen-2-one by reacting with ethyl acetoacetate in the presence of bismuth trichloride which is then oxidized to 2-oxo-2H-benzo[h]chromene-4-carbaldehyde and then condensed with aromatic primary amines to give Schiff bases (3a-3d). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. nema
doi_str_mv 10.2298/JSC111024045M
format article
fullrecord <record><control><sourceid>doaj_cross</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_365fd7356bef48fe8ba7be1b569de1e4</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_365fd7356bef48fe8ba7be1b569de1e4</doaj_id><sourcerecordid>oai_doaj_org_article_365fd7356bef48fe8ba7be1b569de1e4</sourcerecordid><originalsourceid>FETCH-LOGICAL-c187m-d7cf90d2f0d630fe7dad52180e18f0e9f56e547b9ef86e9f8ebbe790efd170f93</originalsourceid><addsrcrecordid>eNpVkE1LAzEURYMoWKtL9_MHRl--JgmupKitVFxU1yGZvGhKOyOTtFB_vdWK4Opy7-JwOYRcUrhizOjrx8WEUgpMgJBPR2RENYNaCUaPyQi4ZLWk3JySs5yXAExKLkbkZrHryjvmlKs-Vqx2n1hSSF3fYa7yxueSyqZgqNp-s3ZD6qqAQ9q6krZ4Tk6iW2W8-M0xeb2_e5lM6_nzw2xyO69bqtW6DqqNBgKLEBoOEVVwQTKqAamOgCbKBqVQ3mDUzb5q9B6VAYyBKoiGj8nswA29W9qPIe2P7Gzvkv0Z-uHNuqGkdoWWNzIGxWXjMQodUXunPFIvGxOQotiz6gOrHfqcB4x_PAr226L9Z5F_AeefZng</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of 2-azetidinones substituted coumarin derivative</title><source>Full-Text Journals in Chemistry (Open access)</source><source>IngentaConnect Journals</source><creator>Mashelkar, Uday ; Jha, Mukesh ; Mashelkar, Beena</creator><creatorcontrib>Mashelkar, Uday ; Jha, Mukesh ; Mashelkar, Beena</creatorcontrib><description>?-Naphthol is converted into 4-methylbenzo[h]chromen-2-one by reacting with ethyl acetoacetate in the presence of bismuth trichloride which is then oxidized to 2-oxo-2H-benzo[h]chromene-4-carbaldehyde and then condensed with aromatic primary amines to give Schiff bases (3a-3d). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. nema</description><identifier>ISSN: 0352-5139</identifier><identifier>EISSN: 1820-7421</identifier><identifier>DOI: 10.2298/JSC111024045M</identifier><language>eng</language><publisher>Serbian Chemical Society</publisher><subject>2-azetidinone ; acid chloride ; aromatic amine ; ethylacetoacetate ; selenium dioxide ; tri-n- butylamine ; α-Naphthol</subject><ispartof>Journal of the Serbian Chemical Society, 2012, Vol.77 (10), p.1339-1344</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c187m-d7cf90d2f0d630fe7dad52180e18f0e9f56e547b9ef86e9f8ebbe790efd170f93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids></links><search><creatorcontrib>Mashelkar, Uday</creatorcontrib><creatorcontrib>Jha, Mukesh</creatorcontrib><creatorcontrib>Mashelkar, Beena</creatorcontrib><title>Synthesis of 2-azetidinones substituted coumarin derivative</title><title>Journal of the Serbian Chemical Society</title><description>?-Naphthol is converted into 4-methylbenzo[h]chromen-2-one by reacting with ethyl acetoacetate in the presence of bismuth trichloride which is then oxidized to 2-oxo-2H-benzo[h]chromene-4-carbaldehyde and then condensed with aromatic primary amines to give Schiff bases (3a-3d). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. nema</description><subject>2-azetidinone</subject><subject>acid chloride</subject><subject>aromatic amine</subject><subject>ethylacetoacetate</subject><subject>selenium dioxide</subject><subject>tri-n- butylamine</subject><subject>α-Naphthol</subject><issn>0352-5139</issn><issn>1820-7421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkE1LAzEURYMoWKtL9_MHRl--JgmupKitVFxU1yGZvGhKOyOTtFB_vdWK4Opy7-JwOYRcUrhizOjrx8WEUgpMgJBPR2RENYNaCUaPyQi4ZLWk3JySs5yXAExKLkbkZrHryjvmlKs-Vqx2n1hSSF3fYa7yxueSyqZgqNp-s3ZD6qqAQ9q6krZ4Tk6iW2W8-M0xeb2_e5lM6_nzw2xyO69bqtW6DqqNBgKLEBoOEVVwQTKqAamOgCbKBqVQ3mDUzb5q9B6VAYyBKoiGj8nswA29W9qPIe2P7Gzvkv0Z-uHNuqGkdoWWNzIGxWXjMQodUXunPFIvGxOQotiz6gOrHfqcB4x_PAr226L9Z5F_AeefZng</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Mashelkar, Uday</creator><creator>Jha, Mukesh</creator><creator>Mashelkar, Beena</creator><general>Serbian Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>2012</creationdate><title>Synthesis of 2-azetidinones substituted coumarin derivative</title><author>Mashelkar, Uday ; Jha, Mukesh ; Mashelkar, Beena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c187m-d7cf90d2f0d630fe7dad52180e18f0e9f56e547b9ef86e9f8ebbe790efd170f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>2-azetidinone</topic><topic>acid chloride</topic><topic>aromatic amine</topic><topic>ethylacetoacetate</topic><topic>selenium dioxide</topic><topic>tri-n- butylamine</topic><topic>α-Naphthol</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mashelkar, Uday</creatorcontrib><creatorcontrib>Jha, Mukesh</creatorcontrib><creatorcontrib>Mashelkar, Beena</creatorcontrib><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of the Serbian Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mashelkar, Uday</au><au>Jha, Mukesh</au><au>Mashelkar, Beena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 2-azetidinones substituted coumarin derivative</atitle><jtitle>Journal of the Serbian Chemical Society</jtitle><date>2012</date><risdate>2012</risdate><volume>77</volume><issue>10</issue><spage>1339</spage><epage>1344</epage><pages>1339-1344</pages><issn>0352-5139</issn><eissn>1820-7421</eissn><abstract>?-Naphthol is converted into 4-methylbenzo[h]chromen-2-one by reacting with ethyl acetoacetate in the presence of bismuth trichloride which is then oxidized to 2-oxo-2H-benzo[h]chromene-4-carbaldehyde and then condensed with aromatic primary amines to give Schiff bases (3a-3d). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. nema</abstract><pub>Serbian Chemical Society</pub><doi>10.2298/JSC111024045M</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0352-5139
ispartof Journal of the Serbian Chemical Society, 2012, Vol.77 (10), p.1339-1344
issn 0352-5139
1820-7421
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_365fd7356bef48fe8ba7be1b569de1e4
source Full-Text Journals in Chemistry (Open access); IngentaConnect Journals
subjects 2-azetidinone
acid chloride
aromatic amine
ethylacetoacetate
selenium dioxide
tri-n- butylamine
α-Naphthol
title Synthesis of 2-azetidinones substituted coumarin derivative
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T13%3A35%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-doaj_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%202-azetidinones%20substituted%20coumarin%20derivative&rft.jtitle=Journal%20of%20the%20Serbian%20Chemical%20Society&rft.au=Mashelkar,%20Uday&rft.date=2012&rft.volume=77&rft.issue=10&rft.spage=1339&rft.epage=1344&rft.pages=1339-1344&rft.issn=0352-5139&rft.eissn=1820-7421&rft_id=info:doi/10.2298/JSC111024045M&rft_dat=%3Cdoaj_cross%3Eoai_doaj_org_article_365fd7356bef48fe8ba7be1b569de1e4%3C/doaj_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c187m-d7cf90d2f0d630fe7dad52180e18f0e9f56e547b9ef86e9f8ebbe790efd170f93%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