20039-93-4Relevant articles and documents
Reductive Aromatization of Quinols with B2pin2 as Deoxidizing Agent
Liu, Bin,Xu, Yin,Luo, Zhibin,Xie, Jimin
supporting information, p. 1022 - 1024 (2020/03/19)
We have demonstrated B2pin2 as superior deoxidizing agent for the reductive deoxygenation of quinol derivatives under basic conditions. A wide range of highly functionalized phenols were obtained in good yields including a complex drug molecule, which revealed the high functional group tolerance of this protocol.
Synthesis, characterization, and reaction of crown ether complexes of aqua(hydroxy)(aryl)iodonium ions
Ochiai, Masahito,Miyamoto, Kazunori,Yokota, Yukie,Suefuji, Takashi,Shiro, Motoo
, p. 75 - 78 (2007/10/03)
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The Nitration of Some Substituted 4-Methylphenols; X-Ray Crystal Structure of (Z)-3-Bromo-5-(bromonitromethylene)furan-2(5H)-one
Gray, Michael J.,Hartshorn, Michael P.,Penfold, Bruce R.,Vaugnan, John
, p. 55 - 64 (2007/10/02)
The nitrations of 2-substituted 4-methyl-6-nitrophenols (1a), (1b) and (1c) give 6-substituted 3-methyl-2-nitro-1,4-benzoquinones (2a), (2b) and (2c).Similar reaction of 2,3-dibromo-4-methyl-6-nitrophenol (5) gives 2,3-dibromo-5-methyl-6-nitro-1,4-benzoquinone (7) and the 4-nitratocyclohexa-2,5-dienone (12).In contrast, 2,3,6-tribromo- (4a) and 2,6-dibromo- (4b) 4-methylphenols give 1,4-benzoquinones with loss of the methyl group.Lactone (18) was formed in the nitration of the 2,6-dibromophenol (4b) and its structure was determined by single-crystal X-ray analysis.