A sequential direct arylation/Suzuki-Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues
Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd 0-coupling approach.
Storr, Thomas E.,Strohmeier, Johanna A.,Baumann, Christoph G.,Fairlamb, Ian J. S.
supporting information; experimental part
p. 6470 - 6472
(2010/10/21)
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