A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues

Thomas E. Storr; Johanna A. Strohmeier; Christoph G. Baumann; Ian J. S. Fairlamb

doi:10.1039/c0cc02043e

A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues

Thomas E. Storr, Johanna A. Strohmeier, Christoph G. Baumann, Ian J. S. Fairlamb

Chemistry of Materials and Catalysis

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

32 Citations (Scopus)

Abstract

Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.

Original language	English
Pages (from-to)	6470-6472
Number of pages	3
Journal	Chemical Communications
Volume	46
Issue number	35
Early online date	17 Aug 2010
DOIs	https://doi.org/10.1039/c0cc02043e
Publication status	Published - 21 Sep 2010

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10.1039/c0cc02043e

Cite this

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title = "A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues",

abstract = "Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.",

author = "Storr, {Thomas E.} and Strohmeier, {Johanna A.} and Baumann, {Christoph G.} and Fairlamb, {Ian J. S.}",

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A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues. / Storr, Thomas E.; Strohmeier, Johanna A.; Baumann, Christoph G.; Fairlamb, Ian J. S.

In: Chemical Communications, Vol. 46, No. 35, 21.09.2010, p. 6470-6472.

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

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AU - Storr, Thomas E.

AU - Strohmeier, Johanna A.

AU - Baumann, Christoph G.

AU - Fairlamb, Ian J. S.

PY - 2010/9/21

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AB - Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.

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EP - 6472

JO - Chemical Communications

JF - Chemical Communications

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