ChemInform Abstract: Synthesis of Hexahydro-1H-benzo[c]chromen-1-amines via the Intramolecular Ring-Opening Reactions of Aziridines by π-Nucleophiles.

ChemInform ◽  
2008 ◽  
Vol 39 (37) ◽  
Author(s):  
Aravinda B. Pulipaka ◽  
Stephen C. Bergmeier
Synthesis ◽  
2021 ◽  
Author(s):  
Angel Ho ◽  
Austin Pounder ◽  
Samuel Koh ◽  
Matthew Macleod ◽  
Emily Carlson ◽  
...  

The present work demonstrates the ability of carboxylic acid-tethered cyclopropanated oxabenzonorbornadienes (CPOBDs) to undergo ring-opening reactions in mild acidic conditions. The optimized reaction conditions involve the use of pTsOH in DCE at 90 °C. Two regioisomers are formed but the reactions are highly regioselective towards type 3 ring-opened products. It was observed that substitution at the C-5 and aryl positions of CPOBD significantly hinders the ring opening reactions leading to decreased yields of ring-opened product, although high regioselectivity for the Type 3 ring-opened product is still maintained. Herein, we report the first examples of acid-catalyzed intramolecular ring-opening reactions of CPOBD with carboxylic acid nucleophiles.


Synlett ◽  
2008 ◽  
Vol 2008 (1) ◽  
pp. 25-28 ◽  
Author(s):  
Richard Grainger ◽  
Richard Boxall ◽  
Caterina Aricò ◽  
Leigh Ferris

2019 ◽  
Vol 60 (45) ◽  
pp. 151228 ◽  
Author(s):  
Christopher Wicks ◽  
Samuel Koh ◽  
Austin Pounder ◽  
Emily Carlson ◽  
William Tam

ChemInform ◽  
2009 ◽  
Vol 40 (12) ◽  
Author(s):  
Xiao-Chun Hang ◽  
Qing-Yun Chen ◽  
Ji-Chang Xiao

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