@Article{Stien+Gastaldi2004,
author="Stien, D.
and Gastaldi, S.",
title="Design of polyaromatic hydrocarbon-supported tin reagents: A new family of tin reagents easily removable from reaction mixtures",
journal="Journal of Organic Chemistry",
year="2004",
publisher="AMER CHEMICAL SOC",
volume="69",
number="13",
pages="4464--4470",
abstract="We report in this paper the preparation and use of stannanes 11, 12a, and 12b, compounds whose 3-pyrenylpropyl side chain affinity for activated carbon simplifies tin removal and product isolation. Our pyrene-supported reagents can be used for radical reductions and cyclizations (11), radical and cationic allylations (12a), and Stille couplings (12b) in much the same way as tributyltin derivatives.",
optnote="ISI:000222187200022",
optnote="exported from refbase (http://php.ecofog.gf/refbase/show.php?record=263), last updated on Wed, 04 May 2011 14:34:58 -0300",
issn="0022-3263"
}