Tetrahedron

Tunable BODIPY derivatives amenable to 'click'and peptide chemistry

…, RH Pedersen, DL Long, N Gadegaard, R Marquez

Index: Hansen, Anna Mette; Sewell, Alan L.; Pedersen, Rasmus H.; Long, De-Liang; Gadegaard, Nikolaj; Marquez, Rodolfo Tetrahedron, 2013 , vol. 69, # 39 p. 8527 - 8533

Full Text: HTML

Citation Number: 10

Abstract

Abstract Novel azido-and amino-functionalised fluorescent probes based on the BODIPY framework have been developed. The probes can be easily and cheaply synthesised, exhibit the highly desirable BODIPY fluorescent properties, and are amenable to 'click'and peptide chemistry methodologies. These probes provide a stable and readily available tool amenable for the visualisation of both solution and solid supported events.

Related Articles:

A new access to pyrrolizidine derivatives: Ring contraction of methyl (E)-[1, 2-oxazin-3-yl] propenoates

[Zimmer, Reinhold; Collas, Markus; Czerwonka, Regina; Hain, Ute; Reissig, Hans-Ulrich Synthesis, 2008 , # 2 p. 237 - 244]

PdII??Catalysed C H Functionalisation of Indoles and Pyrroles Assisted by the Removable N??(2??Pyridyl) sulfonyl Group: C2??Alkenylation and Dehydrogenative …

[Garcia-Rubia, Alfonso; Urones, Beatriz; Arrayas, Ramon Gomez; Carretero, Juan Carlos Chemistry - A European Journal, 2010 , vol. 16, # 31 p. 9676 - 9685]

Synthesis of cystamidin A (pyrrole-3-propanamide), a reported calpain inhibitor

[Bihovsky, Ron; Pendrak, Israil Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 13 p. 1541 - 1542]

Tunable BODIPY derivatives amenable to 'click'and peptide chemistry

[Tetrahedron, , vol. 69, # 39 p. 8527 - 8533]

More Articles...