scholarly journals Correction to Nitrogen–Nitrogen Bond Formation via a Substrate-Bound Anion at a Mononuclear Nickel Platform

2018 ◽  
Vol 37 (6) ◽  
pp. 1086-1086 ◽  
Author(s):  
Mikhail D. Kosobokov ◽  
Aaron Sandleben ◽  
Nicolas Vogt ◽  
Axel Klein ◽  
David A. Vicic
Keyword(s):  
ChemInform ◽  
2010 ◽  
Vol 32 (23) ◽  
pp. no-no
Author(s):  
Sergio Cenini ◽  
Emma Gallo ◽  
Andrea Penoni
Keyword(s):  

Synthesis ◽  
2005 ◽  
Vol 2005 (17) ◽  
pp. 2881-2886 ◽  
Author(s):  
Egle M. Beccalli ◽  
Giorgio Abbiati ◽  
Gianluigi Broggini ◽  
Giuseppe Paladino ◽  
Elisabetta Rossi

Amino Acids ◽  
2008 ◽  
Vol 37 (2) ◽  
pp. 315-321 ◽  
Author(s):  
V. Hahn ◽  
A. Mikolasch ◽  
K. Manda ◽  
D. Gördes ◽  
K. Thurow ◽  
...  
Keyword(s):  

2018 ◽  
Vol 5 (1) ◽  
pp. 18-31
Author(s):  
Seetaram Mohapatra ◽  
Nilofar Baral ◽  
Nilima Priyadarsini Mishra ◽  
Pravati Panda ◽  
Sabita Nayak

Introduction: Aza-Michael addition is an important reaction for carbon-nitrogen bond formation in synthetic organic chemistry. Expalantion: Conjugate addition of imidazole to α,β-unsaturated carbonyl/cyano compounds provides significant numbers of the biologically and synthetically interesting products, such as β-amino acids and β-lactams, which have attracted great attention for their use as key intermediates of anticancer agents, antibiotics and other drugs. Conclusion: This review addresses most significant method for the synthesis of N-substituted imidazole derivatives following Michael addition reaction of imidazole to α,β-unsaturated carbonyl/cyano compounds using ionic liquid/base/acid/enzyme as catalysts from year 2007-2017.


2010 ◽  
Vol 50 (2) ◽  
pp. 507-510 ◽  
Author(s):  
Joachim Ballmann ◽  
Alyssa Yeo ◽  
Brian O. Patrick ◽  
Michael D. Fryzuk
Keyword(s):  

1992 ◽  
Vol 29 (2) ◽  
pp. 283-287 ◽  
Author(s):  
A. Gueiffier ◽  
Y. Blache ◽  
H. Viols ◽  
J. P. Chapat ◽  
O. Chavignon ◽  
...  
Keyword(s):  

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