Font Size:
a
A
A
Keyword [C?H functionalization]
Result: 161 - 180 | Page: 9 of 10
161.
Synthesis Of Nitrogen Heterocycles Via Pd-catalyzed Intermolecular C-H Of Heteroaromatic Compound Addition To Nitriles
162.
Studies On The Selective C?H Functionalization Reactions Of 2,2'-Bipyridyl-6-Carboxamides Catalyzed By Transition Metals
163.
Studies Of Transition-Metal-Catalyzed C-H Functionalization Reaction Of Glycine Derivatives
164.
Studies On The Transition-metal Catalyzed C-H Functionalization To Construct Isoquinoline And 2-Aminoindole Derivatives
165.
Study On C-H Functionalization Of N-Carbamoyl 1,2–Dihydroquinoline Oxidation
166.
Transition Metal Catalyzed Ortho C-H Functionalization Of 2-Arylquinazoline Derivatives
167.
Study On The C
5
-H Bromination Of 8-aminoquinoline Induced By Visible Light Or Electric Reduction
168.
Studies On Transition-metal-catalyzed C-F,C-H Functionalization Abstract
169.
Palladium-Catalyzed C-H Functionalization Promoted By Organophosphorus/Sulphonate Hypervalent-Iodine
170.
Selective [5,5]-Sigmatropic Rearrangement By Assembly Of Aryl Sulfoxides With Allyl Nitriles
171.
Alkylation Of Azoles And Coumarins By C-H Functionalization
172.
The Application Of C-H Bond Functionalization In The Synthesis Of Glycine And Quinoline Derivatives
173.
Boryl Radicals-triggered Selective C-H Functionalization For The Synthesis Of Diverse Phenanthridine Derivatives
174.
Chiral Cyclopentadienyl Rhodium-Catalyzed Enantioselective C-H Functionalization Of Indoles
175.
Study On Conversion Reaction Of 2-diarylindolylmethanols
176.
Cobalt-catalyzed ?-C-H Functionalization Of Ketones And Visible Light Promoted S?H Functionalization Of Thiophenols
177.
Design,Synthesis And Antifungal Bioactivity Of Novel Oxazolines And Analogues
178.
C-H Sulfuration Of Imidazopyridines Using Elemental Sulfur
179.
Enantioselective Synthesis Of Axial Chiral Biaryls By Pd-catalyzed Asymmetric C–H Functionalization
180.
Rh(?)-catalyzed Functionalization Of Ortho-C-H Bond Of 2-Arylquinazolinone
<<First
<Prev
Next>
Last>>
Jump to