7633-56-9Relevant articles and documents
Diaza [1,4] Wittig-type rearrangement of N-allylic-N-Boc-hydrazines into γ-amino- N -Boc-enamines
Tayama, Eiji,Kobayashi, Yoshiaki,Toma, Yuka
supporting information, p. 10570 - 10573 (2016/09/02)
Diaza [1,4] Wittig-type rearrangement of N-allylic-N-Boc-hydrazines into γ-amino-N-Boc-enamines was demonstrated. The scope and limitation, experimental mechanistic studies, and a proposed reaction mechanism were also described.
3-(Hetero)aryl-4-indolylamino-α-tetralones by diastereoselective internal redox cyclization: An "azaenamine" conjugate addition
Ghavtadze, Nugzar,Narayan, Rishikesh,Wibbeling, Birgit,Wuerthwein, Ernst-Ulrich
scheme or table, p. 5185 - 5197 (2011/08/09)
(E)-3-(Hetero)aryl-1-(2-((E)-(indolin-1-ylimino)methyl)phenyl) prop-2-en-1-ones 1 undergo 6-exo-trig cyclization reactions upon treatment with BF3?Me2S in dichloromethane at low temperature to give the tetralones 10 in good yield. Th
TETRACYCLIC INDOLES AS POTASSIUM CHANNEL MODULATORS
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Page/Page column 29, (2008/06/13)
The present invention is directed to compounds of Formula I: that are potassium channel modulators and pharmaceutical compositions thereof. The present invention is further directed to methods of treatment using the compounds and pharmaceutical compositions of the invention. The present invention is still further directed to synthetic processes for producing the compounds of the invention.