72936-38-0Relevant articles and documents
Ketones as electrophile in nitroaldol reaction: Synthesis of β,β-disubstituted-1,3-dinitroalkanes and allylic nitro compounds
Costa, Jeronimo S.,Gomes, Alex O.,Pereira, Vera Lúcia P.,de Souza, Douglas L. F.
, p. 1575 - 1583 (2021/07/06)
β,β-Disubstituted-1,3-dinitro compounds were obtained exclusively with an overall yield of 83% through a domino nitroaldol/elimination/1,4-addition process, when excess nitromethane was added to cyclohexanone or butanone using DBU (1,8-diazabicyclo[5.4.0]
Asymmetric organocatalytic Michael-hemiacetalization reaction: Access to chiral spiro cis-δ-lactones by in situ oxidation of spiro δ-lactols
Wei, Mo-Hui,Zhou, Yi-Rong,Gu, Liang-Hu,Luo, Fan,Zhang, Fang-Lin
supporting information, p. 2546 - 2548 (2013/06/27)
Asymmetric tandem Michael-hemiacetalization reaction between 1-nitromethylcycloalkanol and α,β-unsaturated aldehydes was investigated, which provided an efficient and facile synthesis for spiro cis-δ-lactones by in situ oxidation of spiro δ-lactols in goo
Sulfone substituted imidazo ring ethers
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Page/Page column 46, (2010/11/27)
Imidazo ring compounds (e.g., imidazoquinolines, 6,7,8,9-tetrahydroimidazoquinolines, imidazonaphthyridines, and 6,7,8,9-tetrahydroimidazonaphthyridines) with a sulfide-, sulfinyl-, or sulfonyl-containing ether substituent at the 1-position, pharmaceutica