Dialdehyde + Diamine-Polymer or Macrocycle?
The 24‐membered macrocycle 1 is surprisingly generated from (S)‐2,2′‐dihydroxy‐1,1′‐binaphthyl‐3,3′‐dialdehyde [(S)‐(2)] and (R,R)‐1,2‐diamino‐1,2‐diphenylethane, whereas in the same reaction (R)‐2 yields the polymeric Schiff base as expected. Macrocycle 1 can be used for an economical and simple en...
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Veröffentlicht in: | Angewandte Chemie (International ed.) 1994-01, Vol.33 (1), p.125-126 |
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creator | Brunner, Henri Schiessling, Hubert |
description | The 24‐membered macrocycle 1 is surprisingly generated from (S)‐2,2′‐dihydroxy‐1,1′‐binaphthyl‐3,3′‐dialdehyde [(S)‐(2)] and (R,R)‐1,2‐diamino‐1,2‐diphenylethane, whereas in the same reaction (R)‐2 yields the polymeric Schiff base as expected. Macrocycle 1 can be used for an economical and simple enantiomeric resolution of 2. |
doi_str_mv | 10.1002/anie.199401251 |
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Chem. Int. Ed. Engl</addtitle><description>The 24‐membered macrocycle 1 is surprisingly generated from (S)‐2,2′‐dihydroxy‐1,1′‐binaphthyl‐3,3′‐dialdehyde [(S)‐(2)] and (R,R)‐1,2‐diamino‐1,2‐diphenylethane, whereas in the same reaction (R)‐2 yields the polymeric Schiff base as expected. Macrocycle 1 can be used for an economical and simple enantiomeric resolution of 2.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>0570-0833</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNqFj0tLAzEUhYMoWKtb17NwVzLmMXnMSmqttVJrEUV3ISY3ODp9kAg6_94pI8Wdq8uF852Pg9ApJTklhJ3bVQU5LcuCUCboHupRwSjmSvF91CNCEUw054foKKX3Nq81kT00uKps7eGt8ZANsvZZVivAi3XdLCFm65jdWRfXrnE1XByjg2DrBCe_t4-ersePoxs8u59MR8MZdkxRioOSrZ_qgjOwnrCgrNPMcxWkdV5IT4C4oDlx4Kj0wjkaQHsQBVelgFfeR3nX25pTihDMJlZLGxtDidlONdupZje1Bc46YGOTs3WIduWqtKN4KRmhuo2VXeyrqqH5p9QM59PxXwXu2Cp9wveOtfHDSMWVMM_ziXkoLtXs5ZabBf8BE5Fy7Q</recordid><startdate>19940117</startdate><enddate>19940117</enddate><creator>Brunner, Henri</creator><creator>Schiessling, Hubert</creator><general>Hüthig & Wepf Verlag</general><general>VCH</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19940117</creationdate><title>Dialdehyde + Diamine-Polymer or Macrocycle?</title><author>Brunner, Henri ; Schiessling, Hubert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2711-f7625118432ead02f7ac82d37f6acd56d0e0cf830cec16d5cc1fe8de543795eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brunner, Henri</creatorcontrib><creatorcontrib>Schiessling, Hubert</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Angewandte Chemie (International ed.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brunner, Henri</au><au>Schiessling, Hubert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dialdehyde + Diamine-Polymer or Macrocycle?</atitle><jtitle>Angewandte Chemie (International ed.)</jtitle><addtitle>Angew. Chem. Int. Ed. Engl</addtitle><date>1994-01-17</date><risdate>1994</risdate><volume>33</volume><issue>1</issue><spage>125</spage><epage>126</epage><pages>125-126</pages><issn>0570-0833</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>The 24‐membered macrocycle 1 is surprisingly generated from (S)‐2,2′‐dihydroxy‐1,1′‐binaphthyl‐3,3′‐dialdehyde [(S)‐(2)] and (R,R)‐1,2‐diamino‐1,2‐diphenylethane, whereas in the same reaction (R)‐2 yields the polymeric Schiff base as expected. Macrocycle 1 can be used for an economical and simple enantiomeric resolution of 2.</abstract><cop>Zug</cop><pub>Hüthig & Wepf Verlag</pub><doi>10.1002/anie.199401251</doi><tpages>2</tpages></addata></record> |
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subjects | Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings Organic chemistry Preparations and properties |
title | Dialdehyde + Diamine-Polymer or Macrocycle? |
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