Source:http://linkedlifedata.com/resource/pubmed/id/18540672
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
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pubmed:dateCreated |
2008-6-26
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pubmed:abstractText |
Stereocontrol in the synthesis of dinuclear metal complexes of sulfinylcalix[4]arenes 2 has been achieved by the arrangement of sulfinyl functionalities. Thus, the treatment of the(rtct) isomer of 2 (2(rtct)) with an excess of Et(3)B affords syn dinuclear boron complex 4, while a similar treatment of rctt and rcct isomers 2(rctt) and 2(rcct) yields anti dinuclear complexes 5 and 6, respectively.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2845-8
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pubmed:year |
2008
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pubmed:articleTitle |
Synthesis of dinuclear boron complexes of sulfinylcalix[4]arenes: Syn/Anti stereocontrol by the arrangement of the sulfinyl functions.
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pubmed:affiliation |
Department of Environmental Studies, Graduate School of Environmental Studies, Tohoku University, 6-6-11 Aramaki-Aoba, Aoba-ku, Sendai 980-8579, Japan. morohashi@orgsynth.che.tohoku.ac.jp
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pubmed:publicationType |
Journal Article
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