Synthesis of novel enantiomerically pure trianglimine and trianglamine macrocycles

The synthesis of a series trianglimine macrocycles is described using a [3+3] cyclocondensation strategy between a 1,2-diamine and an aromatic dicarboxaldehyde. The novel compounds have been prepared in enantiomerically pure form and their ring sizes range from 30 to 42. Novel substituted trianglimi...

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Published inTetrahedron: asymmetry Vol. 13; no. 2; pp. 123 - 128
Main Authors Kuhnert, Nikolai, Straßnig, Christian, Lopez-Periago, Ana M.
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 28.02.2002
Elsevier
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Online AccessGet full text
ISSN0957-4166
1362-511X
DOI10.1016/S0957-4166(02)00065-4

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Abstract The synthesis of a series trianglimine macrocycles is described using a [3+3] cyclocondensation strategy between a 1,2-diamine and an aromatic dicarboxaldehyde. The novel compounds have been prepared in enantiomerically pure form and their ring sizes range from 30 to 42. Novel substituted trianglimines are synthesised using a [3+3] cyclocondensation.
AbstractList The synthesis of a series trianglimine macrocycles is described using a [3+3] cyclocondensation strategy between a 1,2-diamine and an aromatic dicarboxaldehyde. The novel compounds have been prepared in enantiomerically pure form and their ring sizes range from 30 to 42. Novel substituted trianglimines are synthesised using a [3+3] cyclocondensation.
The synthesis of a series trianglimine macrocycles is described using a [3+3] cyclocondensation strategy between a 1,2-diamine and an aromatic dicarboxaldehyde. The novel compounds have been prepared in enantiomerically pure form and their ring sizes range from 30 to 42. (C) 2002 Published by Elsevier Science Ltd.
ArticleNumber 0957
Author Kuhnert, Nikolai
Straßnig, Christian
Lopez-Periago, Ana M.
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Snippet The synthesis of a series trianglimine macrocycles is described using a [3+3] cyclocondensation strategy between a 1,2-diamine and an aromatic...
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SubjectTerms Chemistry
Chemistry, Inorganic & Nuclear
Chemistry, Organic
Chemistry, Physical
Physical Sciences
Science & Technology
Title Synthesis of novel enantiomerically pure trianglimine and trianglamine macrocycles
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