Literature DB >> 16733571

The "triamino-analogue" of methyl allocholate; a rigid, functionalised scaffold for supramolecular chemistry.

Khadga M Bhattarai1, Vicente del Amo, Germinal Magro, Adam L Sisson, Jean-Baptiste Joos, Jonathan P H Charmant, Anob Kantacha, Anthony P Davis.   

Abstract

Cholic acid has been converted into triamine with the all-trans polycyclic allocholanoyl skeleton and co-directed, axial amino groups; the potential of this system as a scaffold is illustrated by conversion to a preorganised anion receptor.

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Year:  2006        PMID: 16733571     DOI: 10.1039/b602415g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

Review 1.  Bile acid scaffolds in supramolecular chemistry: the interplay of design and synthesis.

Authors:  Anthony P Davis
Journal:  Molecules       Date:  2007-08-29       Impact factor: 4.411

2.  Triple hybrids of steroids, spiroketals, and oligopeptides as new biomolecular chimeras.

Authors:  Abhisek Banerjee; Eduard Sergienko; Stefan Vasile; Vineet Gupta; Kristiina Vuori; Peter Wipf
Journal:  Org Lett       Date:  2009-01-01       Impact factor: 6.005

  2 in total

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