62260-10-0Relevant academic research and scientific papers
Br?nsted Acid-Initiated Formal [1,3]-Rearrangement Dictated by β-Substituted Ene-Aldimines
Jongwohan, Chanantida,Honda, Yasushi,Suzuki, Toshiyasu,Fujinami, Takeshi,Adachi, Kiyohiro,Momiyama, Norie
supporting information, p. 4991 - 4995 (2019/07/03)
The rearrangement of ene-aldimines is a useful reaction for affording homoallylic amines. Despite their utilities in synthetic chemistry, the rearrangement for accessing homoallylic amines substituted at the 2-position remains elusive. In this study, the
2,2-Diphenyl-5-(4-substituted-piperidino)-3-trans-pentenenitriles
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, (2008/06/13)
This invention encompasses novel 2,2-diphenyl-5-(4-substituted-piperidino)-3-trans-pentenenitriles. These compounds are useful anti-diarrheal agents and also possess analgesic activity.
5-(1,1-Diphenyl-4-(cyclic amino) but-2-trans-en-1-yl)-2-alkyl-1,3,4-oxadiazoles and intermediates thereto
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, (2008/06/13)
This invention encompasses novel 5-[1,1-diphenyl-4-(cyclic amino)but-2-trans-en-1-yl]-2-alkyl-1,3,4-oxadiazoles and intermediates thereto. These compounds are useful anti-diarrheal agents.
