51552-62-6Relevant articles and documents
3-Quinuclidinyl-α-methoxydiphenylacetate: A multi-targeted ligand with antimuscarinic and antinicotinic effects designed for the treatment of anticholinesterase poisoning
Bird, Mike,Gore, Samuel J.,Green, A. Christopher,Lindsay, Christopher D.,Rice, Helen,Tattersall, John E. H.,Timperley, Christopher M.,Whitmore, Charlotte L.
, (2020)
Racemic 3-quinuclidinyl-α-methoxydiphenylacetate (MB266) was synthesised. Its activity at muscarinic acetylcholine receptors (mAChRs), and muscle and neuronal nicotinic acetylcholine receptors (nAChRs), was compared to that of atropine and racemic 3-quinu
Combination of herbicides and safeners
-
, (2008/06/13)
A herbicidally active composition comprises a mixture of A. a herbicidally effective amount of one or more compounds of the formula (I), ?and B. an antidote-effective amount of one or more compounds of the formulae (II) to (IV),
Single and double reductive cleavage of C-O bonds of aromatic dimethyl acetals and ketals: Generation of benzylic mono- and dicarbanions
Azzena,Melloni,Pisano,Sechi
, p. 6759 - 6762 (2007/10/02)
The reductive cleavage of aromatic dimethyl acetals and ketals, 1, with Li metal in THF at low temperature allows the generation of stable α-alkoxy-α-arylsubstituted carbanions, avoiding the Wittig rearrangement. Reaction of these carbanions with various electrophiles afforded the expected products 2. Further in situ reaction of compounds 2 afforded the products of reductive electrophilic disubstitution, 3.