ChemInform Abstract: Palladium-Catalyzed Ring Expansion of Hydroxy Methoxyallenylphthalans as a Novel Synthetic Method for the Highly Substituted 4-Isochromanone Derivatives.

ChemInform ◽  
2010 ◽  
Vol 31 (13) ◽  
pp. no-no
Author(s):  
Ill-Yun Jeong ◽  
Motoo Shiro ◽  
Yoshimitsu Nagao
Synthesis ◽  
2004 ◽  
Vol 2004 (09) ◽  
pp. 1409-1412 ◽  
Author(s):  
Naoki Asao ◽  
Yoshinori Yamamoto ◽  
Kenichiro Sato ◽  
Salprima Yudha S.

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1813
Author(s):  
László Kollár ◽  
Ádám Erdélyi ◽  
Haroon Rasheed ◽  
Attila Takács

The aminocarbonylation of various alkenyl and (hetero)aryl iodides was carried out using tropane-based amines of biological importance, such as 8-azabicyclo[3.2.1]octan-3-one (nortropinone) and 3α-hydroxy-8-azabicyclo[3.2.1]octane (nortropine) as N-nucleophile. Using iodoalkenes, the two nucleophiles were selectively converted to the corresponding amide in the presence of Pd(OAc)2/2 PPh3 catalysts. In the presence of several iodo(hetero)arenes, the application of the bidentate Xantphos was necessary to produce the target compounds selectively. The new carboxamides of varied structure, formed in palladium-catalyzed aminocarbonylation reactions, were isolated and fully characterized. In this way, a novel synthetic method has been developed for the producing of N-acylnortropane derivatives of biological importance.


2011 ◽  
Vol 50 (26) ◽  
pp. 5924-5926 ◽  
Author(s):  
Igor Dubovyk ◽  
Dmitry Pichugin ◽  
Andrei K. Yudin

ChemInform ◽  
2012 ◽  
Vol 43 (52) ◽  
pp. no-no
Author(s):  
Emily B. Corcoran ◽  
Anna B. Williams ◽  
Robert N. Hanson

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