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Published in 2021 at "Journal of Molecular Structure"
DOI: 10.1016/j.molstruc.2021.130861
Abstract: Abstract An efficient, eco-friendly protocol is developed for the synthesis of 1- (α-aminoalkyl)-2-naphthol derivatives via one-pot three-component reaction of 2-naphthol, aromatic aldehydes and piperidine or morpholine in the presence of Amberlite IRA-400 Cl resin as…
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Keywords:
facile synthesis;
synthesis;
synthesis aminoalkyl;
naphthols single ... See more keywords
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Published in 2017 at "Synlett"
DOI: 10.1055/s-0036-1588517
Abstract: N-[(Aminoalkyl)phenyl]-1-naphthamides and N-[(aminoalkyl)phenyl]-5,6,7,8-tetrahydronaphthalene-1-carboxamides were selectively synthesized from the corresponding cyanonaphthamides by catalytic hydrogenation. N-(Amidinophenyl)-1-naphthalenecarboxamides and N-(amidinophenyl)-5,6,7,8-tetrahydronaphthalene-1-carboxamides were chemoselectively obtained from the corresponding O-acetylamidoximes or amidoximes, respectively, by catalytic hydrogenation. The products were screened for their…
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Keywords:
tetrahydronaphthalene carboxamides;
synthesis aminoalkyl;
phenyl;
aminoalkyl amidino ... See more keywords
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Published in 2023 at "Molecules"
DOI: 10.3390/molecules28104067
Abstract: Sclareolide was developed as an efficient C-nucleophilic reagent for an asymmetric Mannich addition reaction with a series of N-tert-butylsulfinyl aldimines. The Mannich reaction was carried out under mild conditions, affording the corresponding aminoalkyl sclareolide derivatives…
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Keywords:
sclareolide derivatives;
antifungal activity;
sclareolide;
synthesis aminoalkyl ... See more keywords