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PMID: 15548077 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Synthesis of rigid multivalent scaffolds based on adamantane.

Organic letters ·Vol. 6 ·No. 24 ·2004-11-25 ·Pages 4567-9

Maison W, Frangioni JV, Pannier N

Abstract

An efficient route to novel 1,3,5,7-tetrasubstituted derivatives of adamantane is described. This route starts from adamantane and gives the tetrafunctionalized derivative 9 in eight steps with an overall yield of 23%. These tetrahedrally shaped molecules possess three identical arms terminated by an activated carboxylic acid derivative and a protected amino function in the 1-position. We propose these tetravalent cage compounds such as 9 as scaffolds for the assembly of ligand/marker conjugates for studies of multivalent ligand receptor interactions. [reaction: see text]

MeSH Terms
Adamantane/chemical synthesis,chemistry Ligands Molecular Conformation
Chemicals
Ligands Adamantane
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Maison Wolfgang
Universität Hamburg, Institut für Organische Chemie, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany. maison@chemie.uni-hamburg.de
Frangioni John V
Pannier Nadine
References (8)
8 references, click to expand
  1. Synthesis of well-defined tower-shaped 1,3,5-trisubstituted adamantanes incorporating a macrocyclic trilactam ring system.
    J Org Chem. 2004 Feb 20;69(4):1010-9 PMID: 14961648
  2. IRDye78 conjugates for near-infrared fluorescence imaging.
    Mol Imaging. 2002 Oct;1(4):354-64 PMID: 12926231
  3. Photochemical preparation of 1,3,5,7-tetracyanoadamantane and its conversion to 1,3,5,7-tetrakis(aminomethyl)adamantane.
    Org Lett. 2004 May 27;6(11):1705-7 PMID: 15151394
  4. Pseudotetrahedral polyhaloadamantanes as chirality probes: synthesis, separation, and absolute configuration.
    J Am Chem Soc. 2002 Nov 13;124(45):13348-9 PMID: 12418863
  5. Nanoscale tripodal 1,3,5,7-tetrasubstituted adamantanes for AFM applications.
    J Org Chem. 2003 Jun 13;68(12):4862-9 PMID: 12790592
  6. Structure-anti-Parkinson activity relationships in the aminoadamantanes. Influence of bridgehead substitution.
    J Med Chem. 1982 Jan;25(1):51-6 PMID: 7086822
  7. Metal-directed formation of three-dimensional M(3)L(2) trigonal-bipyramidal cages.
    Org Lett. 2001 Oct 4;3(20):3141-3 PMID: 11574015
  8. Physicochemical prediction of a brain-blood distribution profile in polycyclic amines.
    Bioorg Med Chem. 2003 Aug 15;11(17):3569-78 PMID: 12901901
Article Info
Journal
Organic letters
Abbr.
Org Lett
ISSN
1523-7060
Published
2004-11-25
Pages
4567-9
Language
English
Region
United States
NLM ID
100890393
PMCID
PMC1421509
Subset
IM
Grants
NCI NIH HHS · R21 CA088245 · United States
NCI NIH HHS · R33 CA088245 · United States
NCI NIH HHS · R21/R33 CA 88245 · United States
NCI NIH HHS · R21 CA 88870 · United States
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