Efficient synthesis of N,N’-methylenebisglycolurils
Coupling of 6-(carboxy)alkyl-2,4-dialkylglycolurils with N-(hydroxymethyl)glycolurils gives N,N’-methylenebisglycolurils totally substituted at the nitrogen atoms, which are formed mostly as racemate diastereomers.
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Published in | Mendeleev communications Vol. 26; no. 2; pp. 136 - 138 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.03.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Coupling of 6-(carboxy)alkyl-2,4-dialkylglycolurils with N-(hydroxymethyl)glycolurils gives N,N’-methylenebisglycolurils totally substituted at the nitrogen atoms, which are formed mostly as racemate diastereomers. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0959-9436 |
DOI: | 10.1016/j.mencom.2016.03.018 |