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  • ...m the ''ortho''- byproduct, and reducing the [[nitro group]] with [[sodium borohydride]]. The resultant [[p-aminophenol|''p''-aminophenol]] is then acetylated wit ...he [[TRPV1]] (older name: vanilloid receptor). Furthermore, AM404 inhibits sodium channels, as do the anesthetics lidocaine and procaine.<ref name="DOI10.100
    54 KB (7,376 words) - 16:52, 27 September 2010
  • ...hydride]] NaBH<sub>4</sub>, under reflux. H<sub>2</sub> is evolved as the borohydride is sequentially converted first to pyrazolylborate [H<sub>3</sub>B(C<sub>3< ...Na<sup>+</sup> HB(mt)<sub>3</sub><sup>-</sup>), [[Methimazole]] and sodium borohydride are heated together.
    9 KB (1,297 words) - 20:14, 21 September 2010
  • ...the NPP intermediate with [[aniline]] followed by reduction with [[sodium borohydride]] affording 4-anilino-''N''-phenethyl-piperidine (ANPP). Finally ANPP and [
    33 KB (4,684 words) - 21:01, 24 September 2010
  • ...he third step the [[ketone]] group is reduced with [[aluminum]] powder and sodium ethoxide in ethanol and quinine can be identified. Quinotoxine is the first ...In the final step the C9 hydroxyl group was introduced by oxidation with [[sodium hydride]], [[dmso]] and oxygen with quinine to epiquinine ratio of 14:1.
    17 KB (2,355 words) - 22:15, 21 September 2010