35572-23-7Relevant articles and documents
Michael-Aldol Double Elimination Cascade to Make Pyridines: Use of Chromone for the Synthesis of Indolizines
Joshi, Dirgha Raj,Kim, Ikyon
, p. 10235 - 10248 (2021)
A domino Michael-aldol double elimination route to indolizines having two different acyl groups at the C5 and C7 positions is described where chromone is employed as a two-carbon unit for the synthesis of a pyridine moiety for the first time. Various analogues were readily accessed in good yields under metal-free and eco-friendly conditions. Further manipulation of the resulting products allowed entry to novel indolizine-heterocycle adducts, which are difficult to access by other methods.
X-ray diffraction and VT-NMR studies of (E)-3-(piperidinyl)-1-(2′-hydroxyphenyl)-prop-2-en-1-one
Choi, Seunghyun,Kim, Yunhye,Park, Bernie Byeonghoon,Park, Suzie,Park, Jonghyun,Ok, Kiwon,Koo, Jaehyung,Jung, Yong Woo,Jeon, Young Ho,Lee, Eun Hee,Lee, Ken S.,Byun, Youngjoo
, p. 600 - 605 (2015/02/19)
A series of 1-aryl-3-(cyclicamino)-prop-2-en-1-one analogs was synthesized from commercial acetophenones in 2 or 3 steps. Compound 6, (E)-3-(piperidinyl)-1-(2′-hydroxyphenyl)-prop-2-en-1-one, exhibited the unique shape and intensity of the Csp2
Benzopyrans: Part XIX - Reactions of 3-Acetyl- and 3-Acetyl-2-methyl-4-oxo-4H-benzopyrans with Nitrogen Nucleophiles
Ghosh, Chandra Kanta,Pal, Chandana,Bhattacharyya, Atanu
, p. 914 - 917 (2007/10/02)
3-Acetyl-4-oxo-4H-benzopyran (1a) gives with piperidine the enaminoketone (2); with phenylhydrazine a mixture of the pyrazoles (5a and 7a, R'=Ph); and with hydroxylamine the nitrile (12) and isoxazole (13a) under two different conditions.Like 1a, the chromenone (1b) also behaves as a Michael acceptor towards hydrazine and hydroxylamine to produce the pyrazoles (7b, R'=H, Ph) and isoxazole (13b), respectively.Guanidine forms the pyrimidine (17a) with 1a, but 18b with 1b.