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1.
Org Lett ; 20(3): 620-623, 2018 02 02.
Artículo en Inglés | MEDLINE | ID: mdl-29360377

RESUMEN

A simple and efficient protocol for silver(I)-catalyzed picolinamide directed C4-H amination of 1-naphthylamine derivatives with readily available azodicarboxylates has been developed, demonstrating a new approach to 1,4-naphthalenediamine derivatives in high yields. Note that this reaction system could proceed under external-oxidant- and additive-free conditions (only requires 5 mol % of AgOAc as the catalyst in acetone).

2.
J Org Chem ; 82(23): 12119-12127, 2017 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-29039195

RESUMEN

A mild and efficient protocol for C4-H sulfonylation of 1-naphthylamine derivatives with sodium sulfinates has been described. This C4 sulfonylation proceeded smoothly at room temperature under Ru/Cu photoredox catalysis or Cu/Ag cocatalysis and could tolerate various functional groups. In addition, control experiments suggested that this C4-H sulfonylation reaction might proceed via a single-electron-transfer process.

3.
Org Lett ; 18(18): 4594-7, 2016 09 16.
Artículo en Inglés | MEDLINE | ID: mdl-27584840

RESUMEN

A simple and facile protocol for palladium-catalyzed picolinamide-directed C8-H amination of 1-naphthylamine derivatives with simple secondary aliphatic amines was developed, thereby providing a new route to 1,8-naphthalenediamine derivatives. It is noteworthy that the picolinamide moiety as a bidentate directing group may play a key role in this regioselective transformation.

4.
Org Lett ; 17(24): 6086-9, 2015 Dec 18.
Artículo en Inglés | MEDLINE | ID: mdl-26629979

RESUMEN

A simple and mild protocol for copper(I)-mediated sulfonylation of 8-aminoquinoline amides with sulfonyl chlorides was developed, affording desired products in moderate to good yields. This reaction proceeds in air and features excellent substrate tolerance, especially for aliphatic sulfonyl chlorides.

5.
Org Biomol Chem ; 13(8): 2432-6, 2015 Feb 28.
Artículo en Inglés | MEDLINE | ID: mdl-25569834

RESUMEN

An efficient and generally applicable protocol for palladium-catalyzed oxidative deacetonative coupling of 4-aryl-2-methyl-3-butyn-2-ols with dialkyl H-phosphonates has been developed. This methodology provides a new and practical route to alkynylphosphonates using the inexpensive 4-aryl-2-methyl-3-butyn-2-ols as the alkyne sources. This reaction could also be performed with aryl bromides, 2-methyl-3-butyne-2-ol and dialkyl H-phosphonates using the cheap 2-methyl-3-butyne-2-ol as an alkyne source.


Asunto(s)
Butanoles/química , Compuestos Organometálicos/química , Organofosfonatos/química , Paladio/química , Catálisis , Estructura Molecular , Oxidación-Reducción
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