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1.
J Org Chem ; 80(18): 9354-9, 2015 Sep 18.
Artículo en Inglés | MEDLINE | ID: mdl-26334559

RESUMEN

A new domino Heck-isomerization/Saegusa/Heck reaction of propenol with aryl iodides has been developed for the synthesis of 3,3-diaryl propenals by triple transition-metal catalysis. Moreover, we also developed the domino Heck-isomerization/Heck-type reaction of propenol with aryl iodides for the synthesis of 1,3-diaryl propanones by double transition-metal catalysis and the mediation of secondary amine or triple transition metal catalysis and aminocatalysis.

2.
Org Biomol Chem ; 13(15): 4466-72, 2015 Apr 21.
Artículo en Inglés | MEDLINE | ID: mdl-25773505

RESUMEN

A novel DCC reaction between aromatic aldehydes or ketones and H-phosphonates has been developed for the synthesis of p-formyl or p-acylphenylphosphonates. The synthetic method has excellent para regioselectivities, good yields, and broad substrate scopes and is more benign to the environment. The DCC reaction also tolerates many functional groups, and results in a series of new p-formyl and p-acylphenylphosphonates, which should be important building blocks for the synthesis of versatile arylphosphonate derivatives.


Asunto(s)
Aldehídos/química , Hidrocarburos Aromáticos/química , Cetonas/química , Organofosfonatos/química , Acilación , Aldehídos/síntesis química , Formiatos/síntesis química , Formiatos/química , Hidrocarburos Aromáticos/síntesis química , Cetonas/síntesis química , Organofosfonatos/síntesis química , Estereoisomerismo
3.
Artículo en Zh | WPRIM | ID: wpr-234393

RESUMEN

<p><b>OBJECTIVE</b>To study a Chinese pedigree with Hailey-Hailey disease (HHD) and identify the ATP2C1 gene mutation in this family.</p><p><b>METHODS</b>All exons of the ATP2C1 gene were analyzed with polymerase chain reaction and DNA sequencing in all patients of this family and 80 unrelated population-matched controls.</p><p><b>RESULTS</b>We identified a nonsense mutation 163C to T, resulting in a premature termination codon in ATP2C1 gene. The mutation was not found in normal individuals of the family and controls.</p><p><b>CONCLUSION</b>The mutation can affect the result of transcription and translation of ATP2C1 gene, and it is firstly reported in the Chinese pedigree with HHD.</p>


Asunto(s)
Humanos , Pueblo Asiatico , Genética , ATPasas Transportadoras de Calcio , Genética , Análisis Mutacional de ADN , Linaje , Pénfigo Familiar Benigno , Genética
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