Dual Function Catalysts. Dehydrogenation and Asymmetric Intramolecular Diels−Alder Cycloaddition ofN-Hydroxy Formate Esters and Hydroxamic Acids:  Evidence for a Ruthenium−Acylnitroso Intermediate

2005 ◽  
Vol 127 (11) ◽  
pp. 3678-3679 ◽  
Author(s):  
Chun P. Chow ◽  
Kenneth J. Shea
2011 ◽  
Vol 13 (13) ◽  
pp. 3442-3445 ◽  
Author(s):  
Duangduan Chaiyaveij ◽  
Leah Cleary ◽  
Andrei S. Batsanov ◽  
Todd B. Marder ◽  
Kenneth J. Shea ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (45) ◽  
pp. no-no
Author(s):  
Duangduan Chaiyaveij ◽  
Leah Cleary ◽  
Andrei S. Batsanov ◽  
Todd B. Marder ◽  
Kenneth J. Shea ◽  
...  

2010 ◽  
Vol 7 (6) ◽  
pp. 475-478 ◽  
Author(s):  
Ahmad Fakhruddin ◽  
Kesiny Phomkeona ◽  
Abdel-Moneim Abu-Elfotoh ◽  
Kazutaka Shibatomi ◽  
Seiji Iwasa

2018 ◽  
Vol 14 ◽  
pp. 531-536 ◽  
Author(s):  
Hisato Shimizu ◽  
Akira Yoshimura ◽  
Keiichi Noguchi ◽  
Victor N Nemykin ◽  
Viktor V Zhdankin ◽  
...  

[Bis(trifluoroacetoxy)iodo]benzene (BTI) and (diacetoxyiodo)benzene (DIB) efficiently promote the formation of acylnitroso species from hydroxamic acids in the presence of various dienes to give the corresponding hetero-Diels–Alder (HDA) adducts in moderate to high yields. The present method could be applied to the HDA reactions of acylnitroso species witho-benzoquinones generated by the oxidative dearomatization of guaiacols.


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