ChemInform Abstract: Facile One-Pot Synthesis of Poly-Substituted Phenols from Baylis-Hillman Adducts via [4 + 2] Annulation Protocol.

ChemInform ◽  
2008 ◽  
Vol 39 (34) ◽  
Author(s):  
Seong Jin Kim ◽  
Sung Hwan Kim ◽  
Ko Hoon Kim ◽  
Jae Nyoung Kim
2020 ◽  
Vol 44 (12) ◽  
pp. 4834-4841
Author(s):  
Ali Rahmatpour

Regioselective synthesis of a series of novel diaryl- and naphthyl-fused 2,8-dioxabicyclo[3.3.2]nonanes was accomplished by a one-pot reaction of p-substituted phenols and 2-naphthol with 2,5-dimethoxytetrahydrofuran.


2020 ◽  
Author(s):  
Lucien Caspers ◽  
Julian Spils ◽  
Mattis Damrath ◽  
Enno Lork ◽  
Boris Nachtsheim

In this article we describe an efficient approach for the synthesis of cyclic diaryliodonium salts. The method is based on benzyl alcohols as starting materials and consists of an Friedel-Crafts-arylation/oxidation sequence. Besides a deep optimization, particluar focusing on the choice and ratios of the utilized Bronsted-acids and oxidants, we explore the substrate scope of this transformation. We also discuss an interesting isomerism of cyclic iodonium salts substituted with aliphatic substituents at the bridge head carbon. <br>


2017 ◽  
Vol 7 (12) ◽  
pp. 1192-1195
Author(s):  
Y. I. Shaikh ◽  
G. M. Nazeruddin ◽  
Khursheed Ahmed

2013 ◽  
Vol 30 (6) ◽  
pp. 636-642
Author(s):  
Xueli Zhang ◽  
Zhilan Lin ◽  
Huiling Hu ◽  
Jiaxin He ◽  
Yuan Gao

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