23602-61-1Relevant articles and documents
Extending the stetter reaction with 1,6-acceptors
Law, Katherine R.,McErlean, Christopher S. P.
supporting information, p. 15852 - 15855 (2014/04/03)
Pace Stetter: A new N-heterocyclic carbene (NHC)-catalysed transformation is described-the intramolecular vinylogous Stetter reaction. This transformation can be effected with both thiazolium and triazolium-based catalysts, using aromatic and aliphatic aldehydes, employing α,β,γ,δ- unsaturated esters, ketones, phosphonates and N-acylpyrroles, and can be conducted enantioselectively (see scheme). Copyright
CHEMICAL COMPOUNDS
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Page/Page column 27, (2008/12/04)
This invention relates to non-steroidal compounds that are modulators of androgen receptor, and also to the methods for the making and use of such compounds.
Salicylaldoxime moiety as a phenolic "A-ring" substitute in estrogen receptor ligands
Minutolo,Bertini,Papi,Carlson,Katzenellenbogen,Macchia
, p. 4288 - 4291 (2007/10/03)
The phenolic "A-ring" of natural and synthetic estrogen receptor (ER) ligands was effectively replaced by a planar six-member ring formed through an intramolecular hydrogen bond within a salicylaldoxime. Thus, oxime 1, a structural analogue of a triarylet
Design, synthesis, and monoamine transporter binding site affinities of methoxy derivatives of indatraline
Gu,Yu,Jacobson,Rothman,Dersch,George,Flippen-Anderson,Rice
, p. 4868 - 4876 (2007/10/03)
A series of methoxy-containing derivatives of indatraline 13a-f and 17 were synthesized, and their binding affinities for the dopamine, serotonin, and norepinephrine transporter binding sites were determined. Introduction of a methoxy group to indatraline