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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...
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Published in: | Journal of the Serbian Chemical Society 2012, Vol.77 (10), p.1339-1344 |
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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 |
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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.
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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> |
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language | eng |
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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 |
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