Synthesis of Enantiopure Chiral Perhydrobenzimidazole and Hexahydroquinoxaline Derivatives

Starting from 2-anilino-2-ethoxy-3-oxothiobutyric acid anilides and (R, R)-or (S, S)-trans-1,2-diaminocyclohexane, chiral C2-disubstituted perhydrobenzimidazole and trans-4a,5,6,7,8,8a-hexahydroquinoxaline derivatives were obtained depending on the polarity of the solvent.

Saved in:
Bibliographic Details
Published in:Monatshefte für Chemie 2000-10, Vol.131 (10), p.1061-1066
Main Authors: Zaleska, Barbara, Socha, Robert
Format: Article
Language:English
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-c263t-9c688535a5b7aa3cd5ff48265d62d6c8cd3487b2d294270e78e8ae3023580c993
cites
container_end_page 1066
container_issue 10
container_start_page 1061
container_title Monatshefte für Chemie
container_volume 131
creator Zaleska, Barbara
Socha, Robert
description Starting from 2-anilino-2-ethoxy-3-oxothiobutyric acid anilides and (R, R)-or (S, S)-trans-1,2-diaminocyclohexane, chiral C2-disubstituted perhydrobenzimidazole and trans-4a,5,6,7,8,8a-hexahydroquinoxaline derivatives were obtained depending on the polarity of the solvent.
doi_str_mv 10.1007/s007060070038
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2899099004</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2899099004</sourcerecordid><originalsourceid>FETCH-LOGICAL-c263t-9c688535a5b7aa3cd5ff48265d62d6c8cd3487b2d294270e78e8ae3023580c993</originalsourceid><addsrcrecordid>eNpVUMFKAzEUDKJgrR69Bzyvvk2y2exRam2FgoJ68bKkyVuask1qsi1tv96t9SI85vF4w8wwhNzmcJ8DlA-pB5BHAK7OyCAXXGRClMU5GQAwmVVMlJfkKqUl9LcAPiBf73vfLTC5RENDx177zoX1JiIdLVzULX3DuNjbGOboD27lrD6EFqn2lk5xp39f3xvnw063ziN9wui2unNbTNfkotFtwpu_PSSfz-OP0TSbvU5eRo-zzDDJu6wyUqmCF7qYl1pzY4umEYrJwkpmpVHGcqHKObOsEqwELBUqjRwYLxSYquJDcnfSXR-jYOrqZdhE31vWTFUV9AOiZ2UnlokhpYhNvY5upeO-zqE-1lf_q4__ACo2Yz4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2899099004</pqid></control><display><type>article</type><title>Synthesis of Enantiopure Chiral Perhydrobenzimidazole and Hexahydroquinoxaline Derivatives</title><source>Springer Link</source><creator>Zaleska, Barbara ; Socha, Robert</creator><creatorcontrib>Zaleska, Barbara ; Socha, Robert</creatorcontrib><description>Starting from 2-anilino-2-ethoxy-3-oxothiobutyric acid anilides and (R, R)-or (S, S)-trans-1,2-diaminocyclohexane, chiral C2-disubstituted perhydrobenzimidazole and trans-4a,5,6,7,8,8a-hexahydroquinoxaline derivatives were obtained depending on the polarity of the solvent.</description><identifier>ISSN: 0026-9247</identifier><identifier>EISSN: 1434-4475</identifier><identifier>DOI: 10.1007/s007060070038</identifier><language>eng</language><publisher>Heidelberg: Springer Nature B.V</publisher><ispartof>Monatshefte für Chemie, 2000-10, Vol.131 (10), p.1061-1066</ispartof><rights>Springer-Verlag/Wien 2000.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c263t-9c688535a5b7aa3cd5ff48265d62d6c8cd3487b2d294270e78e8ae3023580c993</citedby></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>Zaleska, Barbara</creatorcontrib><creatorcontrib>Socha, Robert</creatorcontrib><title>Synthesis of Enantiopure Chiral Perhydrobenzimidazole and Hexahydroquinoxaline Derivatives</title><title>Monatshefte für Chemie</title><description>Starting from 2-anilino-2-ethoxy-3-oxothiobutyric acid anilides and (R, R)-or (S, S)-trans-1,2-diaminocyclohexane, chiral C2-disubstituted perhydrobenzimidazole and trans-4a,5,6,7,8,8a-hexahydroquinoxaline derivatives were obtained depending on the polarity of the solvent.</description><issn>0026-9247</issn><issn>1434-4475</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNpVUMFKAzEUDKJgrR69Bzyvvk2y2exRam2FgoJ68bKkyVuask1qsi1tv96t9SI85vF4w8wwhNzmcJ8DlA-pB5BHAK7OyCAXXGRClMU5GQAwmVVMlJfkKqUl9LcAPiBf73vfLTC5RENDx177zoX1JiIdLVzULX3DuNjbGOboD27lrD6EFqn2lk5xp39f3xvnw063ziN9wui2unNbTNfkotFtwpu_PSSfz-OP0TSbvU5eRo-zzDDJu6wyUqmCF7qYl1pzY4umEYrJwkpmpVHGcqHKObOsEqwELBUqjRwYLxSYquJDcnfSXR-jYOrqZdhE31vWTFUV9AOiZ2UnlokhpYhNvY5upeO-zqE-1lf_q4__ACo2Yz4</recordid><startdate>20001001</startdate><enddate>20001001</enddate><creator>Zaleska, Barbara</creator><creator>Socha, Robert</creator><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20001001</creationdate><title>Synthesis of Enantiopure Chiral Perhydrobenzimidazole and Hexahydroquinoxaline Derivatives</title><author>Zaleska, Barbara ; Socha, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c263t-9c688535a5b7aa3cd5ff48265d62d6c8cd3487b2d294270e78e8ae3023580c993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zaleska, Barbara</creatorcontrib><creatorcontrib>Socha, Robert</creatorcontrib><collection>CrossRef</collection><jtitle>Monatshefte für Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zaleska, Barbara</au><au>Socha, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Enantiopure Chiral Perhydrobenzimidazole and Hexahydroquinoxaline Derivatives</atitle><jtitle>Monatshefte für Chemie</jtitle><date>2000-10-01</date><risdate>2000</risdate><volume>131</volume><issue>10</issue><spage>1061</spage><epage>1066</epage><pages>1061-1066</pages><issn>0026-9247</issn><eissn>1434-4475</eissn><abstract>Starting from 2-anilino-2-ethoxy-3-oxothiobutyric acid anilides and (R, R)-or (S, S)-trans-1,2-diaminocyclohexane, chiral C2-disubstituted perhydrobenzimidazole and trans-4a,5,6,7,8,8a-hexahydroquinoxaline derivatives were obtained depending on the polarity of the solvent.</abstract><cop>Heidelberg</cop><pub>Springer Nature B.V</pub><doi>10.1007/s007060070038</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0026-9247
ispartof Monatshefte für Chemie, 2000-10, Vol.131 (10), p.1061-1066
issn 0026-9247
1434-4475
language eng
recordid cdi_proquest_journals_2899099004
source Springer Link
title Synthesis of Enantiopure Chiral Perhydrobenzimidazole and Hexahydroquinoxaline Derivatives
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T07%3A58%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20Enantiopure%20Chiral%20Perhydrobenzimidazole%20and%20Hexahydroquinoxaline%20Derivatives&rft.jtitle=Monatshefte%20f%C3%BCr%20Chemie&rft.au=Zaleska,%20Barbara&rft.date=2000-10-01&rft.volume=131&rft.issue=10&rft.spage=1061&rft.epage=1066&rft.pages=1061-1066&rft.issn=0026-9247&rft.eissn=1434-4475&rft_id=info:doi/10.1007/s007060070038&rft_dat=%3Cproquest_cross%3E2899099004%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c263t-9c688535a5b7aa3cd5ff48265d62d6c8cd3487b2d294270e78e8ae3023580c993%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2899099004&rft_id=info:pmid/&rfr_iscdi=true