A New and Efficient Method foro-Quinone Methide Intermediate Generation:  Application to the Biomimetic Synthesis of (±)-Alboatrin

2004 ◽  
Vol 6 (20) ◽  
pp. 3617-3619 ◽  
Author(s):  
Raphaël Rodriguez ◽  
Robert M. Adlington ◽  
John E. Moses ◽  
Andrew Cowley ◽  
Jack E. Baldwin
ChemInform ◽  
2005 ◽  
Vol 36 (4) ◽  
Author(s):  
Raphael Rodriguez ◽  
Robert M. Adlington ◽  
John E. Moses ◽  
Andrew Cowley ◽  
Jack E. Baldwin

Synlett ◽  
2018 ◽  
Vol 29 (11) ◽  
pp. 1517-1519 ◽  
Author(s):  
Thomas Pettus ◽  
Zhen-Gao Feng ◽  
G. Burnett

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.


2014 ◽  
Vol 50 (39) ◽  
pp. 5053-5056 ◽  
Author(s):  
Takuya Oguma ◽  
Tsutomu Katsuki

A tandem combination of ortho-quinone methide (o-QM) formation/Michael addition/asymmetric dearomatization, which is catalysed by an iron–salan complex in air with high enantioselectivity, provides an efficient method for spirocyclic (2H)-dihydrobenzofuran synthesis from 2-naphthols and phenols.


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