Loading…

One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines

Abstract A novel one-pot synthesis of polysubstituted oxa(thia)zolidin-2-imines has been developed. It employs A 3 -coupling of aldehyde and amine with alkyne to form propargyl amine, which on (thio)amidation with iso(thio)cyanate produces N -propargyl(thio)urea, and a cyclization reaction. A 5- exo...

Full description

Saved in:
Bibliographic Details
Published in:Synlett 2012-08, Vol.23 (13), p.1955-1959
Main Authors: Madaan, Chetna, Saraf, Shuddham, Priyadarshani, Garima, Reddy, P. Purushotham, Guchhait, Sankar K., Kunwar, A. C., Sridhar, B.
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-c307t-177730a77f6356fcf6bd603029e11f963b5fa9f3c3e0a6a0856d1cb8dc44712a3
cites
container_end_page 1959
container_issue 13
container_start_page 1955
container_title Synlett
container_volume 23
creator Madaan, Chetna
Saraf, Shuddham
Priyadarshani, Garima
Reddy, P. Purushotham
Guchhait, Sankar K.
Kunwar, A. C.
Sridhar, B.
description Abstract A novel one-pot synthesis of polysubstituted oxa(thia)zolidin-2-imines has been developed. It employs A 3 -coupling of aldehyde and amine with alkyne to form propargyl amine, which on (thio)amidation with iso(thio)cyanate produces N -propargyl(thio)urea, and a cyclization reaction. A 5- exo -dig iodocyclization of N -propargylurea constructs 5-iodomethyleneoxazolidin-2-imine, while cycloisomerization of the thio analogue provides 5-methylenethiazolidin-2-imine. In this process, CuI catalysis has been found to be crucial, and the cyclization occurs through oxygen/sulfur (not nitrogen) nucleophilic attack to alkyne.
doi_str_mv 10.1055/s-0032-1316606
format article
fullrecord <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_0032_1316606</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_0032_1316606</sourcerecordid><originalsourceid>FETCH-LOGICAL-c307t-177730a77f6356fcf6bd603029e11f963b5fa9f3c3e0a6a0856d1cb8dc44712a3</originalsourceid><addsrcrecordid>eNp1kEFLwzAYhoMoOKdXz70ICmb70rRpe5ThVBhs6DyXNE1YRpuUJFW3X2_HhjdPH7y8zwvfg9AtgQmBNJ16DEBjTChhDNgZGpGEZjiGgp2jERSU4TQmySW68n4LQJK8gBH6XhqJVzY8RuuNkxJ_BNlFM9t10uEZD7zZ7WUdzfWXxNO57YfQtp010oToXXIRtDVD3fjgehF8tLLNzveVDzr0YQCXP_x-vdH8YW8bXWuDY6xbbaS_RheKN17enO4Yfc6f17NXvFi-vM2eFlhQyAImWZZR4FmmGE2ZEopVNQMKcSEJUQWjVap4oaigEjjjkKesJqLKa5EkGYk5HaPJcVc4672TquycbrnblQTKg7bSlwdt5UnbANwdgY57wRvluBHa_1Exi0mRs3To4WMvbLRsZbkd5Jjhk_92fwFqKXvv</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines</title><source>Thieme - Connect here FIRST to enable access</source><creator>Madaan, Chetna ; Saraf, Shuddham ; Priyadarshani, Garima ; Reddy, P. Purushotham ; Guchhait, Sankar K. ; Kunwar, A. C. ; Sridhar, B.</creator><creatorcontrib>Madaan, Chetna ; Saraf, Shuddham ; Priyadarshani, Garima ; Reddy, P. Purushotham ; Guchhait, Sankar K. ; Kunwar, A. C. ; Sridhar, B.</creatorcontrib><description>Abstract A novel one-pot synthesis of polysubstituted oxa(thia)zolidin-2-imines has been developed. It employs A 3 -coupling of aldehyde and amine with alkyne to form propargyl amine, which on (thio)amidation with iso(thio)cyanate produces N -propargyl(thio)urea, and a cyclization reaction. A 5- exo -dig iodocyclization of N -propargylurea constructs 5-iodomethyleneoxazolidin-2-imine, while cycloisomerization of the thio analogue provides 5-methylenethiazolidin-2-imine. In this process, CuI catalysis has been found to be crucial, and the cyclization occurs through oxygen/sulfur (not nitrogen) nucleophilic attack to alkyne.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-0032-1316606</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><subject>Chemistry ; Exact sciences and technology ; Heterocyclic compounds ; Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms ; Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives ; letter ; Organic chemistry ; Preparations and properties</subject><ispartof>Synlett, 2012-08, Vol.23 (13), p.1955-1959</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c307t-177730a77f6356fcf6bd603029e11f963b5fa9f3c3e0a6a0856d1cb8dc44712a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0032-1316606.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0032-1316606$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3017,3018,27924,27925,54559,54560</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26219865$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Madaan, Chetna</creatorcontrib><creatorcontrib>Saraf, Shuddham</creatorcontrib><creatorcontrib>Priyadarshani, Garima</creatorcontrib><creatorcontrib>Reddy, P. Purushotham</creatorcontrib><creatorcontrib>Guchhait, Sankar K.</creatorcontrib><creatorcontrib>Kunwar, A. C.</creatorcontrib><creatorcontrib>Sridhar, B.</creatorcontrib><title>One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract A novel one-pot synthesis of polysubstituted oxa(thia)zolidin-2-imines has been developed. It employs A 3 -coupling of aldehyde and amine with alkyne to form propargyl amine, which on (thio)amidation with iso(thio)cyanate produces N -propargyl(thio)urea, and a cyclization reaction. A 5- exo -dig iodocyclization of N -propargylurea constructs 5-iodomethyleneoxazolidin-2-imine, while cycloisomerization of the thio analogue provides 5-methylenethiazolidin-2-imine. In this process, CuI catalysis has been found to be crucial, and the cyclization occurs through oxygen/sulfur (not nitrogen) nucleophilic attack to alkyne.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms</subject><subject>Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives</subject><subject>letter</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kEFLwzAYhoMoOKdXz70ICmb70rRpe5ThVBhs6DyXNE1YRpuUJFW3X2_HhjdPH7y8zwvfg9AtgQmBNJ16DEBjTChhDNgZGpGEZjiGgp2jERSU4TQmySW68n4LQJK8gBH6XhqJVzY8RuuNkxJ_BNlFM9t10uEZD7zZ7WUdzfWXxNO57YfQtp010oToXXIRtDVD3fjgehF8tLLNzveVDzr0YQCXP_x-vdH8YW8bXWuDY6xbbaS_RheKN17enO4Yfc6f17NXvFi-vM2eFlhQyAImWZZR4FmmGE2ZEopVNQMKcSEJUQWjVap4oaigEjjjkKesJqLKa5EkGYk5HaPJcVc4672TquycbrnblQTKg7bSlwdt5UnbANwdgY57wRvluBHa_1Exi0mRs3To4WMvbLRsZbkd5Jjhk_92fwFqKXvv</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>Madaan, Chetna</creator><creator>Saraf, Shuddham</creator><creator>Priyadarshani, Garima</creator><creator>Reddy, P. Purushotham</creator><creator>Guchhait, Sankar K.</creator><creator>Kunwar, A. C.</creator><creator>Sridhar, B.</creator><general>Georg Thieme Verlag</general><general>Thieme</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20120801</creationdate><title>One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines</title><author>Madaan, Chetna ; Saraf, Shuddham ; Priyadarshani, Garima ; Reddy, P. Purushotham ; Guchhait, Sankar K. ; Kunwar, A. C. ; Sridhar, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-177730a77f6356fcf6bd603029e11f963b5fa9f3c3e0a6a0856d1cb8dc44712a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms</topic><topic>Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives</topic><topic>letter</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Madaan, Chetna</creatorcontrib><creatorcontrib>Saraf, Shuddham</creatorcontrib><creatorcontrib>Priyadarshani, Garima</creatorcontrib><creatorcontrib>Reddy, P. Purushotham</creatorcontrib><creatorcontrib>Guchhait, Sankar K.</creatorcontrib><creatorcontrib>Kunwar, A. C.</creatorcontrib><creatorcontrib>Sridhar, B.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Madaan, Chetna</au><au>Saraf, Shuddham</au><au>Priyadarshani, Garima</au><au>Reddy, P. Purushotham</au><au>Guchhait, Sankar K.</au><au>Kunwar, A. C.</au><au>Sridhar, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>23</volume><issue>13</issue><spage>1955</spage><epage>1959</epage><pages>1955-1959</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract A novel one-pot synthesis of polysubstituted oxa(thia)zolidin-2-imines has been developed. It employs A 3 -coupling of aldehyde and amine with alkyne to form propargyl amine, which on (thio)amidation with iso(thio)cyanate produces N -propargyl(thio)urea, and a cyclization reaction. A 5- exo -dig iodocyclization of N -propargylurea constructs 5-iodomethyleneoxazolidin-2-imine, while cycloisomerization of the thio analogue provides 5-methylenethiazolidin-2-imine. In this process, CuI catalysis has been found to be crucial, and the cyclization occurs through oxygen/sulfur (not nitrogen) nucleophilic attack to alkyne.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0032-1316606</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0936-5214
ispartof Synlett, 2012-08, Vol.23 (13), p.1955-1959
issn 0936-5214
1437-2096
language eng
recordid cdi_crossref_primary_10_1055_s_0032_1316606
source Thieme - Connect here FIRST to enable access
subjects Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
letter
Organic chemistry
Preparations and properties
title One-Pot, Three-Step Copper-Catalyzed Five-/Four-Component Reaction Constructs Polysubstituted Oxa(Thia)zolidin-2-imines
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T16%3A31%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=One-Pot,%20Three-Step%20Copper-Catalyzed%20Five-/Four-Component%20Reaction%20Constructs%20Polysubstituted%20Oxa(Thia)zolidin-2-imines&rft.jtitle=Synlett&rft.au=Madaan,%20Chetna&rft.date=2012-08-01&rft.volume=23&rft.issue=13&rft.spage=1955&rft.epage=1959&rft.pages=1955-1959&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/s-0032-1316606&rft_dat=%3Cthieme_cross%3E10_1055_s_0032_1316606%3C/thieme_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c307t-177730a77f6356fcf6bd603029e11f963b5fa9f3c3e0a6a0856d1cb8dc44712a3%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