Synthesis of α-monobrominated pyrrole derivatives

Article abstract of DOI:10.1080/00397919508011772

Surprisingly stable N-t-BOC-2-bromo-4-hexyl-pyrrole is prepared from N-t-BOC-2-trimethylstannyl-4-hexyl-pyrrole using N-bromosuccinimide as reagent. The bromo-stannyl exchange reaction is performed quantitatively in THF at -70°C under inert atmosphere. Si

Full text of DOI:10.1080/00397919508011772

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Synthetic Communications: An
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Synthesis of α-Monobrominated
Pyrrole Derivatives
L. Groenendaal a , M. E. Van Loo a , J. A. J. M. Vekemans a &
E. W. Meijer a
a Laboratory of Organic Chemistry Eindhoven University
of Technology, P.O. Box 513, 5600, MB Eindhoven, The
Netherlands
Version of record first published: 23 Sep 2006.
To cite this article: L. Groenendaal , M. E. Van Loo , J. A. J. M. Vekemans & E. W. Meijer
(1995): Synthesis of α-Monobrominated Pyrrole Derivatives, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry, 25:10,
1589-1600
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