One-pot annulation to tricyclo[5.3.1.03,8]undecane-2,6-diones by sequential three-fold Michael reactions. A formal synthesis of (±)-seychellene

Author(s):  
Hisahiro Hagiwara ◽  
Akihiro Okano ◽  
Hisashi Uda
2020 ◽  
Vol 2020 (15) ◽  
pp. 2264-2270 ◽  
Author(s):  
Antonio Macchia ◽  
Valentina Dafnae Cuomo ◽  
Antonia Di Mola ◽  
Giovanni Pierri ◽  
Consiglia Tedesco ◽  
...  
Keyword(s):  
One Pot ◽  

2016 ◽  
Vol 358 (10) ◽  
pp. 1602-1607 ◽  
Author(s):  
Wusheng Guo ◽  
Victor Laserna ◽  
Jeroen Rintjema ◽  
Arjan W. Kleij
Keyword(s):  
One Pot ◽  

ChemInform ◽  
2005 ◽  
Vol 36 (2) ◽  
Author(s):  
Wengui Wang ◽  
Marvin Yu
Keyword(s):  
One Pot ◽  

2016 ◽  
Vol 14 (1) ◽  
pp. 259-264 ◽  
Author(s):  
Sherida Johnson ◽  
Fujie Tanaka

C-glycosides were synthesized from unprotected 2-N-acyl-aldohexoses and unactivated ketones in one pot via aldol condensation–oxa-Michael reactions.


2014 ◽  
Vol 16 (4) ◽  
pp. 2111-2116 ◽  
Author(s):  
Jennifer J. Lee ◽  
George A. Kraus

Diverse functionalized aromatic compounds including DMT are constructed from captodative dienophiles with exclusive regioselectivity.


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