A Direct Approach to 5-Hydroxybenzofurans via a Platinum-Catalyzed Domino Rearrangement/5-endo-dig Cyclization Reaction of Quinols
摘要:
A highly efficient and atom-economical construction of 2-substituted 5-hydroxybenzofurans was accomplished by employing a platinum-catalyzed domino dienone-phenol rearrangement/5-endo-dig cyclization reaction of quinols bearing alkynes.
STERN, ALAN J.;SWENTON, JOHN S., J. ORG. CHEM., 53,(1988) N 11, 2465-2468
作者:STERN, ALAN J.、SWENTON, JOHN S.
DOI:——
日期:——
A Direct Approach to 5-Hydroxybenzofurans via a Platinum-Catalyzed Domino Rearrangement/5-<i>endo</i>-<i>dig</i> Cyclization Reaction of Quinols
作者:Ikyon Kim、Kyungsun Kim、Jungeun Choi
DOI:10.1021/jo901937u
日期:2009.11.6
A highly efficient and atom-economical construction of 2-substituted 5-hydroxybenzofurans was accomplished by employing a platinum-catalyzed domino dienone-phenol rearrangement/5-endo-dig cyclization reaction of quinols bearing alkynes.
Addition of organolithium reagents to quinone silyl methyl monoketals. A useful expedient in the synthesis of p-quinols having acid-sensitive groups