71127-36-1Relevant academic research and scientific papers
Efficient synthesis of t-butyl 3-alkyl-N-hydroxy-oxindole-3-carboxylates from di-t-butyl 2-nitrophenylmalonates
Yamai, Yu-suke,Ishida, Kyoji,Natsutani, Itaru,Uesato, Shinichi,Nagaoka, Yasuo,Sumiyoshi, Takaaki
, p. 1257 - 1268 (2019/07/31)
– A selective and efficient synthesis of t-butyl 3-alkyl-N-hydroxy-oxindole-3-carboxylates from di-t-butyl 2-nitrophenylmalonates is described. A tandem reduction-cyclization approach involving reduction of di-t-butyl 2-methyl-(2-nitrophenyl)malonate to d
Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation
Ueno, Masahiro,Yonemoto, Misato,Hashimoto, Masahiro,Wheatley, Andrew E. H.,Naka, Hiroshi,Kondo, Yoshinori
, p. 2264 - 2266 (2008/01/03)
A novel type of deprotonative arylation of nucleophiles was conducted using Et3SiH/cat. t-Bu-P4 and the powerful SNAr reactions of aryl fluorides were accomplished using alcohols and malonates as nucleophiles. The Royal Society of Ch
