Carbon-Nitrogen Bond Formation by Reductive Elimination from Nickel(II) Amido Alkyl Complexes

1995 ◽  
Vol 14 (9) ◽  
pp. 4421-4423 ◽  
Author(s):  
Kwangmo Koo ◽  
Gregory L. Hillhouse
Keyword(s):  
Bond Formation ◽  
Reductive Elimination ◽  
Alkyl Complexes ◽  
Nitrogen Bond

ChemInform Abstract: Carbon-Nitrogen Bond Formation Catalyzed by Metalloporphyrins

ChemInform ◽  
2010 ◽  
Vol 32 (23) ◽  
pp. no-no
Author(s):  
Sergio Cenini ◽  
Emma Gallo ◽  
Andrea Penoni
Keyword(s):  
Bond Formation ◽  
Nitrogen Bond

Diverse mechanisms of carbon-hydrogen bond formation through binuclear reductive elimination reactions

1982 ◽  
Vol 104 (2) ◽  
pp. 619-621 ◽  
Author(s):  
Mario J. Nappa ◽  
Roberto Santi ◽  
Steven P. Diefenbach ◽  
Jack Halpern
Keyword(s):  
Hydrogen Bond ◽  
Bond Formation ◽  
Reductive Elimination ◽  
Hydrogen Bond Formation ◽  
Elimination Reactions

A Valuable Synthesis of Pyrrolo[1,2-a]quinoxalines, Indolo[1,2-a]quinoxalines and their Aza-Analogues by Palladium-Catalyzed Intramolecular Carbon-Nitrogen Bond Formation

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

Laccase-catalyzed carbon–nitrogen bond formation: coupling and derivatization of unprotected l-phenylalanine with different para-hydroquinones

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

scholarly journals Carbon(sp3)-nitrogen bond-forming reductive elimination from phosphine-ligated alkylpalladium(II) amide complexes: A DFT study

Tetrahedron ◽  
2019 ◽  
Vol 75 (2) ◽  
pp. 137-143 ◽  
Author(s):  
Quan Jiang ◽  
D. Matthew Peacock ◽  
John F. Hartwig ◽  
Thomas R. Cundari
Keyword(s):  
Reductive Elimination ◽  
Dft Study ◽  
Bond Forming ◽  
Nitrogen Bond

scholarly journals Michael Addition of Imidazole to α, β -Unsaturated Carbonyl/Cyano Compound

2018 ◽  
Vol 5 (1) ◽  
pp. 18-31
Author(s):  
Seetaram Mohapatra ◽  
Nilofar Baral ◽  
Nilima Priyadarsini Mishra ◽  
Pravati Panda ◽  
Sabita Nayak
Keyword(s):  
Organic Chemistry ◽  
Amino Acids ◽  
Anticancer Agents ◽  
Michael Addition ◽  
Addition Reaction ◽  
Bond Formation ◽  
Conjugate Addition ◽  
Michael Addition Reaction ◽  
Cyano Compounds ◽  
Nitrogen Bond

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.

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