scholarly journals Enantioselective Organocatalytic Syntheses and Ring‐Expansions of Cyclobutane Derivatives

2021 ◽  
Vol 2021 (21) ◽  
pp. 3023-3034
Author(s):  
Manuel Barday ◽  
Pierre Bouillac ◽  
Yoann Coquerel ◽  
Muriel Amatore ◽  
Thierry Constantieux ◽  
...  
Synlett ◽  
2021 ◽  
Author(s):  
Memg Wang ◽  
Changxu Zhong ◽  
Ping Lu

Enantioselective synthesis of cyclobutane derivatives is still a challenging topic in asymmetric synthesis. [2+2]-Cycloaddition and skeleton rearrangement are two primary strategies to this end. Recently, functionalization of cyclobutanones and cyclobutenones, which are readily available via [2+2]-cycloadditions as prochiral substrates, has emerged as a powerful tool to access versatile four-membered ring compounds. Herein, we summarize some recent advances in these areas from our and other groups.


1981 ◽  
Vol 22 (18) ◽  
pp. 1701-1704 ◽  
Author(s):  
Mikio Hori ◽  
Tadashi Kataoka ◽  
Hiroshi Shimizu ◽  
Norihiro Ueda
Keyword(s):  

1967 ◽  
Vol 45 (23) ◽  
pp. 2933-2942 ◽  
Author(s):  
Seyhan N. Ege ◽  
Peter Yates

Ultraviolet irradiation of 3-(p-anisyl)-2-cyclohexenone and 3-(p-nitrophenyl)-2-cyclohexenone has been found to give a single photodimer in each case, the structures of which have been established as the cis–anti–cis head-to-head cyclobutane derivatives XI and XIII, respectively.


ChemInform ◽  
2010 ◽  
Vol 26 (15) ◽  
pp. no-no
Author(s):  
W. ZHANG ◽  
Y. HUA ◽  
S. J. GEIB ◽  
G. HOGE ◽  
P. DOWD
Keyword(s):  

ChemInform ◽  
2010 ◽  
Vol 30 (10) ◽  
pp. no-no
Author(s):  
Sylvie Piva-Le Blanc ◽  
Sandrine Henon ◽  
Olivier Piva

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