Copper-catalyzed oxidative esterification of aldehydes with dialkyl peroxides: efficient synthesis of esters of tertiary alcohols

RSC Advances ◽  
2013 ◽  
Vol 3 (33) ◽  
pp. 13668 ◽  
Author(s):  
Yefeng Zhu ◽  
Yunyang Wei
Keyword(s):  
Efficient Synthesis ◽  
Oxidative Esterification ◽  
Tertiary Alcohols ◽  
Dialkyl Peroxides

Iron-Nitrate-Catalyzed Oxidative Esterification of Aldehydes and Alcohols with N -Hydroxyphthalimide: Efficient Synthesis of N -Hydroxyimide Esters

2017 ◽  
Vol 2017 (47) ◽  
pp. 7160-7166 ◽  
Author(s):  
Xiaohe Xu ◽  
Jian Sun ◽  
Yuyan Lin ◽  
Jingya Cheng ◽  
Pingping Li ◽  
...  
Keyword(s):  
Iron Nitrate ◽  
Efficient Synthesis ◽  
Oxidative Esterification

Direct Access to α-Acyloxycarbonyl Compounds and Esters via Oxidative Esterification of Aldehydes under Visible Light

2021 ◽  
Author(s):  
Anindita Bhowmick ◽  
Prakash K Warghude ◽  
Pankaj D Dharpure ◽  
Ramakrishna G. Bhat
Keyword(s):  
Visible Light ◽  
Benzyl Bromide ◽  
Direct Access ◽  
Efficient Synthesis ◽  
Oxidative Esterification

Herein we report the efficient synthesis of α-acyloxycarbonyl compounds and esters starting directly from aldehydes and α-bromocarbonyl compounds/benzyl bromide derivatives and bromo nitriles using an organic photocatalyst in combination with...

Efficient synthesis of an α-trifluoromethyl-α-tosyloxymethyl epoxide enabling stepwise double functionalisation to afford CF3-substituted tertiary alcohols

2008 ◽  
Vol 49 (34) ◽  
pp. 5101-5104 ◽  
Author(s):  
Steven P. Keeling ◽  
Ian B. Campbell ◽  
Diane M. Coe ◽  
Tony W.J. Cooper ◽  
George W. Hardy ◽  
...  
Keyword(s):  
Efficient Synthesis ◽  
Tertiary Alcohols

scholarly journals Synthesis of enantiomerically pure N-(2,3-dihydroxypropyl)arylamides via oxidative esterification

2013 ◽  
Vol 9 ◽  
pp. 2129-2136 ◽  
Author(s):  
Akula Raghunadh ◽  
Satish S More ◽  
T Krishna Chaitanya ◽  
Yadla Sateesh Kumar ◽  
Suresh Babu Meruva ◽  
...  
Keyword(s):  
Ring Opening ◽  
Efficient Synthesis ◽  
Enantiomerically Pure ◽  
Step Process ◽  
Oxidative Esterification ◽  
Highly Efficient ◽  
Chiral Purity ◽  
High Yields ◽  
Nitrogen Heterocyclic

A highly efficient synthesis of enantiomerically pure (S) and (R)-isomers of N-(2,3-dihydroxypropyl)arylamides has been developed with good overall yields in a two step process. The key step involves the ring opening of the chiral epoxide with a nitrogen heterocyclic carbene (NHC) and further rearrangement to chiral N-(2,3-dihydroxypropyl)arylamides in high yields and enantioselectivity. During the reaction, no erosion in chiral purity was observed.

A new facile and efficient synthesis of trans-(+)-sobrerol by biotransformation of α-pinene using extremophiles microorganisms

Planta Medica ◽  
2009 ◽  
Vol 75 (09) ◽  
Author(s):  
LA Vilaseca ◽  
J Quillaguamán ◽  
L Fuentes ◽  
O Sterner
Keyword(s):  
Efficient Synthesis
Sign in / Sign up

Export Citation Format

Share Document