Novel Synthesis of 3-Substituted 2,3-Dihydrobenzofurans via ortho-Quinone Methide Intermediates Generated in Situ

2014 ◽  
Vol 16 (5) ◽  
pp. 1478-1481 ◽  
Author(s):  
Abdul kadar Shaikh ◽  
George Varvounis
Synlett ◽  
2018 ◽  
Vol 29 (07) ◽  
pp. 912-917 ◽  
Author(s):  
Parviz Ranjbar ◽  
Narjes Rezaei ◽  
Ehsan Sheikhi

A metal-free oxidative C(sp3)–N coupling process has been developed for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones. The reaction between primary amines, isatoic anhydride, and benzylic alcohols in the presence of HBr in DMSO at 80 °C affords 2,3-dihydroquinazolin-4(1H)-ones in excellent yields. Under these reaction conditions, benzylic alcohols react with in situ generated bromodimethylsulfonium bromide to form alkoxysulfonium intermediates. These intermediates undergo an oxidative cyclization reaction with primary amines and isatoic anhydride to produce the title products.


RSC Advances ◽  
2015 ◽  
Vol 5 (98) ◽  
pp. 80212-80215 ◽  
Author(s):  
N. J. Willis ◽  
C. D. Bray
Keyword(s):  

A method for the generation/in situhetero-Diels–Alder cycloaddition of a trisubstitutedortho-quinone methide (o-QM) is described.


2015 ◽  
Vol 3 (32) ◽  
pp. 16513-16519 ◽  
Author(s):  
Liyuan Zhang ◽  
Hui Huang ◽  
Hailin Yin ◽  
Yang Xia ◽  
Jianmin Luo ◽  
...  

A novel synthesis of graphene–sulfur composites is designed by electrolytic exfoliation of graphite coupled with in situ electrodeposition of sulfur.


RSC Advances ◽  
2015 ◽  
Vol 5 (19) ◽  
pp. 14892-14896 ◽  
Author(s):  
Abdul kadar Shaikh ◽  
George Varvounis

A simple and efficient one-pot cascade reaction for the regioselective synthesis of trans or cis/trans-2,3-disubstituted 2,3-dihydrobenzofurans, is described.


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