Convenient synthesis of substituted tetrahydrofuran via Lewis base catalyzed [3 + 2] domino reactions

RSC Advances ◽  
2014 ◽  
Vol 4 (95) ◽  
pp. 52629-52632 ◽  
Author(s):  
Yufen Liu ◽  
Qi Zhang ◽  
Yanlong Du ◽  
Aimin Yu ◽  
Kui Zhang ◽  
...  

A DABCO catalyzed domino reaction between 3-oxo-4-(2-oxoindolin-3-ylidene) butanoates and allenoates furnished 2,3,5-substituted tetrahydrofuran furan derivatives bearing oxindole moiety and two exocyclic double bonds in high yield.

ChemInform ◽  
2015 ◽  
Vol 46 (16) ◽  
pp. no-no
Author(s):  
Yufen Liu ◽  
Qi Zhang ◽  
Yanlong Du ◽  
Aimin Yu ◽  
Kui Zhang ◽  
...  

2020 ◽  
Vol 56 (3) ◽  
pp. 443-445 ◽  
Author(s):  
Masumi Itazaki ◽  
Takanari Matsutani ◽  
Tomoya Nochida ◽  
Toshiyuki Moriuchi ◽  
Hiroshi Nakazawa

Convenient synthesis of phosphinecarboxamidein by hydrophosphination of isocyanates (and isothiocyanates) was achieved without catalyst and solvent. This system shows shorter reaction time, high yield, and good functional group tolerance.


ChemInform ◽  
2010 ◽  
Vol 41 (2) ◽  
Author(s):  
Xueming Chen ◽  
Hui Wei ◽  
Yunyun Chen ◽  
Xingshu Li

2020 ◽  
Vol 22 (18) ◽  
pp. 6137-6147
Author(s):  
Yahui Gong ◽  
Pingzhou Wang ◽  
Cai Wu ◽  
Jie Wang ◽  
Chun Shen

Upgrading aqueous acetone–butanol–ethanol mixtures to high-density bio-fuels is realized via the three-step domino reaction in a green way.


2011 ◽  
Vol 7 ◽  
pp. 1182-1188
Author(s):  
Abhishek Santra ◽  
Anup Kumar Misra

A convenient synthesis of the tetrasaccharide repeating unit of theO-antigen ofShigella boydiitype 9 has been achieved in excellent yield using a [2 + 2] block glycosylation strategy. TEMPO-mediated selective oxidation of the primary alcohol of the tetrasaccharide derivative8to the carboxylic group followed by deprotection of the functional groups furnished target tetrasaccharide1as its 4-methoxyphenyl glycoside in high yield.


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