Organocatalyzed solvent-free aza-Henry reaction: a breakthrough in the one-pot synthesis of 1,2-diamines.
J Org Chem
; 69(23): 8168-71, 2004 Nov 12.
Article
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| MEDLINE
| ID: mdl-15527316
ABSTRACT
A nitrogen-containing superbase such as TMG was found to be an effective catalyst for the reaction between N-diphenylphosphinoyl imines and nitroalkanes. Exploiting a protocol that avoids the use of any solvent also during workup procedure, we synthesized a series of beta-nitroamines in excellent yields and high diastereomeric ratios. These results, combined with the capability of the indium in conjunction with Zn as the stoichiometric reducing agent to perform in aqueous medium reduction of the nitro group under mild reaction conditions, led us to devise a three-step, one-pot synthesis of a range of 1,2-diamines, making use of environmentally friendly procedures in the various steps.
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Banco de datos:
MEDLINE
Idioma:
En
Revista:
J Org Chem
Año:
2004
Tipo del documento:
Article
País de afiliación:
Italia