29476-10-6

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 536-74-3 phenylacetylene 
• 333-27-7 methyl trifluoromethanesulfonate 
• 5667-03-8 2-phenylbenzo[b][1,4]thiazepin-4(5H)-one 
• 637-44-5 phenylpropyolic acid 
• 137-07-5 2-amino-benzenethiol 
• 29476-08-2 2-phenyl-4-methylthio-1,5-benzothiazepine 
• 624-84-0 formic acid hydrazide 

Relevant academic research and scientific papers

Alkyltriflate-triggered annulation of arylisothiocyanates and alkynes leading to multiply substituted quinolines through domino electrophilic activation

The reaction of arylisothiocyanate, alkyltriflate, and alkynes leads to variously substituted quinolines in high yields. The reaction undergoes alkyltriflate-triggered domino electrophilic activation and avoids the use of a transition-metal catalyst. A variety of functional groups are tolerated in the quinoline ring.

Studies of annelated 1,4-benzothiazines and 1,5-benzothiazepines. VII. Synthesis and inhibition of benzodiazepine receptor binding of some 4,5-dihydro-tetrazolo[5,1-d]-1,5-benzothiazepines and 5-phenyl-s-triazolo[3,4-d]-1,5-benzothiazepines

The 4,5-dihydro-tetrazolo[5,1-d]-1,5-benzothiazepines 3a-k and the 5-phenyl-s-triazolo[3,4-d]-1,5-benzothiazepines 6a-f and 11a-c have been prepared and tested for their ability to displace [H] flunitrazepam binding from bovine brain membranes. Some of th