Nucleotide base recognition: Synthesis of artificial receptors containing two distinct binding regions for the complexation of bis-thymine derivatives

Andrew D. Hamilton; Dorothy Little

doi:10.1039/C39900000297

Nucleotide base recognition: Synthesis of artificial receptors containing two distinct binding regions for the complexation of bis-thymine derivatives

Andrew D. Hamilton, Dorothy Little

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Oxidative coupling of a propargyloxy-substituted, diamidopyridine-based receptor for thymine leads to a new dimeric receptor that shows strong binding to bis-thymine derivatives.

Original language	English (US)
Pages (from-to)	297-300
Number of pages	4
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	4
DOIs	https://doi.org/10.1039/C39900000297
State	Published - 1990

ASJC Scopus subject areas

Molecular Medicine

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title = "Nucleotide base recognition: Synthesis of artificial receptors containing two distinct binding regions for the complexation of bis-thymine derivatives",

abstract = "Oxidative coupling of a propargyloxy-substituted, diamidopyridine-based receptor for thymine leads to a new dimeric receptor that shows strong binding to bis-thymine derivatives.",

author = "Hamilton, {Andrew D.} and Dorothy Little",

year = "1990",

doi = "10.1039/C39900000297",

language = "English (US)",

pages = "297--300",

journal = "Journal of the Chemical Society, Chemical Communications",

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publisher = "Royal Society of Chemistry",

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Nucleotide base recognition: Synthesis of artificial receptors containing two distinct binding regions for the complexation of bis-thymine derivatives

Abstract

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