N-Heterocyclic carbenes derived from imidazo-[1,5-a]pyridines related to natural products: synthesis, structure and potential biological activity of some corresponding gold(I) and silver(I) complexes

2016 ◽  
Vol 30 (7) ◽  
pp. 581-589 ◽  
Author(s):  
Monica Mihorianu ◽  
M Heiko Franz ◽  
Peter G Jones ◽  
Matthias Freytag ◽  
Gerhard Kelter ◽  
...  
Keyword(s):  
Natural Products ◽  
Biological Activity ◽  
Heterocyclic Carbenes ◽  
Potential Biological Activity ◽  
Natural Products Synthesis

ChemInform Abstract: Exploring Chemical Diversity of Epoxyquinoid Natural Products: Synthesis and Biological Activity of (-)-Jesterone and Related Molecules.

ChemInform ◽  
2010 ◽  
Vol 32 (38) ◽  
pp. no-no
Author(s):  
Yongbo Hu ◽  
Chaomin Li ◽  
Bheemashankar A. Kulkarni ◽  
Gary Strobel ◽  
Emil Lobkovsky ◽  
...  
Keyword(s):  
Natural Products ◽  
Biological Activity ◽  
Chemical Diversity ◽  
Natural Products Synthesis

Exploring Chemical Diversity of Epoxyquinoid Natural Products:  Synthesis and Biological Activity of (−)-Jesterone and Related Molecules

2001 ◽  
Vol 3 (11) ◽  
pp. 1649-1652 ◽  
Author(s):  
Yongbo Hu ◽  
Chaomin Li ◽  
Bheemashankar A. Kulkarni ◽  
Gary Strobel ◽  
Emil Lobkovsky ◽  
...  
Keyword(s):  
Natural Products ◽  
Biological Activity ◽  
Chemical Diversity ◽  
Natural Products Synthesis

scholarly journals Nitroso Diels–Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products

2014 ◽  
Vol 12 (38) ◽  
pp. 7445-7468 ◽  
Author(s):  
Serena Carosso ◽  
Marvin J. Miller
Keyword(s):  
Natural Products ◽  
Biological Activity ◽  
Diels Alder ◽  
Efficient Tool ◽  
Potential Biological Activity

This review describes the use of nitroso Diels–Alder reactions for the functionalization of complex diene-containing natural products in order to generate libraries of compounds with potential biological activity.

scholarly journals Recent advances of N-heterocyclic carbenes in the applications of constructing carbo- and heterocyclic frameworks with potential biological activity

RSC Advances ◽  
2021 ◽  
Vol 11 (60) ◽  
pp. 38060-38078
Author(s):  
Mei-Mei Li ◽  
Xiaozhen Chen ◽  
Yun Deng ◽  
Jun Lu
Keyword(s):  
Biological Activity ◽  
Heterocyclic Carbenes ◽  
General Picture ◽  
Potential Biological Activity ◽  
Recent Advances

A general picture of utilization of NHCs in constructing several kinds of bioactive cyclic skeletons.

Recent applications of asymmetric organocatalytic annulation reactions in natural product synthesis

2021 ◽  
Author(s):  
Nengzhong Wang ◽  
Zugen Wu ◽  
Junjie Wang ◽  
Nisar Ullah ◽  
Yixin Lu
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Natural Product Synthesis ◽  
Natural Products Synthesis

A comprehensive and updated summary of asymmetric organocatalytic annulation reactions is presented; in particular, the applications of these annulation strategies to natural products synthesis are highlighted.

scholarly journals Synthesis of α-Aminophosphonates and Related Derivatives; The Last Decade of the Kabachnik–Fields Reaction

Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2511
Author(s):  
Petra R. Varga ◽  
György Keglevich
Keyword(s):  
Biological Activity ◽  
Solvent Free ◽  
Trialkyl Phosphite ◽  
Catalyst Free ◽  
Potential Biological Activity

The Kabachnik–Fields reaction, comprising the condensation of an amine, oxo compound and a P-reagent (generally a >P(O)H species or trialkyl phosphite), still attracts interest due to the challenging synthetic procedures and the potential biological activity of the resulting α-aminophosphonic derivatives. Following the success of the first part (Molecules 2012, 17, 12821), here we summarize the synthetic developments in this field accumulated in the last decade. The procedures compiled include catalytic accomplishments as well as catalyst-free and/or solvent-free “greener” protocols. The products embrace α-aminophosphonates, α-aminophosphinates, and α-aminophosphine oxides along with different bis derivatives from the double phospha-Mannich approach. The newer developments of the aza-Pudovik reactions are also included.

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