13161-32-5Relevant articles and documents
A Biomimetic Synthesis of des -Hydroxy Paecilospirone
Feng, Zhen-Gao,Burnett, G. Leslie,Pettus, Thomas R. R.
supporting information, p. 1517 - 1519 (2018/05/16)
The carbon framework of des -hydroxy paecilospirone was rapidly synthesized using a biomimetic approach whereby an enol ether and an ortho -quinone methide (o- QM), each derived from the same lactone, were combined to arrive at the complete carbon skeleton of paecilospirone.
Regiocontrolled rearrangement of isobenzofurans
Egan, Ben A.,Paradowski, Michael,Thomas, Lynne H.,Marquez, Rodolfo
supporting information; experimental part, p. 2086 - 2089 (2011/06/25)
Regioselective alkylation and oxidative rearrangement of isobenzofurans has been achieved to generate substituted 4,8- ihydroxyisochromanones in good yields and with complete regiocontrol.
Facile Interconversion of the Isomeric Acid Chlorides Derived from Half Methyl Esters of 3-Methoxyphthalic Acid
Gupta, Dahmendra N.,Hodge, Philip,Hurley, Peter N.
, p. 391 - 394 (2007/10/02)
The isomeric acid chlorides obtained by treating the half methyl esters of 3-methoxyphthalic acid with thionyl chloride interconvert so readily that it is not practical to isolate one acid chloride free of the other.At equilibrium the main isomer is the a