135145-84-5

Upstream product

• 93296-09-4 4-methoxyphenylzinc chloride 
• 135145-81-2 3,4,6-tri-O-triisopropylsilyl-1-iodo-D-glucal 
• 131216-80-3 1,5-anhydro-2-desoxy-3,4,6-tri-O-triisopropylsilyl-1-(tri-n-butyl-stannyl)-D-arabino-hex-1-enitol 
• 131216-78-9 1,5-anhydro-2-desoxy-3,4,6-tri-O-triisopropylsilyl-D-arabino-hex-1-enitol 
• 696-62-8 para-iodoanisole 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 5720-07-0 4-methoxyphenylboronic acid 

Relevant academic research and scientific papers

Palladium-catalyzed cross-coupling reactions between dihydropyranylindium reagents and aryl halides. Synthesis of C-aryl glycals

(Matrix presented) Palladium(0)-catalyzed cross-coupling reactions between tris(dihydropyranyl)indium 1 and aryl halides 2 have been investigated. Aryl iodides and electron-deficient aryl bromides couple efficiently with the in situ-generated indium reage

The preparation of C-aryl glucals via palladium-catalyzed cross-coupling methods

The C-aryl glucals 17-31 have been prepared by the palladium-catalyzed cross coupling of 1-tributylstannyl-3,4,6-tri-O-(tert-butyldimethylsilyl)-b-glucal (11) and aryl bromides. The major by-product in all of these reactions is the dimer 33, the product o

Preparation of C-Aryl Glucals via the Palladium-Catalyzed Coupling of Metalated Aromatics with 1-Iodo-3,4,6-tri-O-(triisopropylsilyl)-D-glucal

The preparation of the novel iodo glucal 5 from 3,4,6-tri-O-(triisopropylsilyl)-D-glucal (4), via a two-step procedure involving C1 stannylation and subsequent tin-iodine exchange, is described.The palladium-catalyzed coupling of 5 with a variety of metal