21071-24-9Relevant articles and documents
Straightforward Synthesis of Fluorinated Enals via Photocatalytic α-Perfluoroalkenylation of Aldehydes
Wulkesch, Christian,Czekelius, Constantin
, p. 7425 - 7438 (2021/06/21)
(Per)fluorinated substances represent an important compound class with regard to drug design and material chemistry. We found a mild, operationally simple, and inexpensive photocatalytic perfluoroalkenylation reaction giving tetrasubstituted, highly electron-deficient enals straight from aldehydes. This one-step reaction tolerates various functional groups and can be applied to a wide range of substrates giving the products in yields of 52-84%.
Design, synthesis, and evaluation of no-donor containing carbonic anhydrase inhibitors to lower intraocular pressure
Huang, Qinhua,Rui, Eugene Y.,Cobbs, Morena,Dinh, Dac M.,Gukasyan, Hovhannes J.,Lafontaine, Jennifer A.,Mehta, Saurabh,Patterson, Brian D.,Rewolinski, David A.,Richardson, Paul F.,Edwards, Martin P.
, p. 2821 - 2833 (2015/04/14)
The antiglaucoma drugs dorzolamide (1) and brinzolamide (2) lower intraocular pressure (IOP) by inhibiting the carbonic anhydrase (CA) enzyme to reduce aqueous humor production. The introduction of a nitric oxide (NO) donor into the alkyl side chain of do
18O assisted analysis of a γ,δ-epoxyketone cyclization: Synthesis of the C16-C28 fragment of ammocidin D
Chau, Stephen T.,Hayakawa, Yoichi,Sulikowski, Gary A.
supporting information; experimental part, p. 756 - 759 (2011/04/24)
The C16-C28 fragment common to the cytotoxic macrolide ammocidin D has been prepared by a stereospecific 5-exo closure of a γ,δ-epoxyketone followed by a rearrangement to a pyran acetal. The reaction pathway was traced by 18O labeling of the ke