Y Wu, W Lu, YN Ma, F Chen, W Ren… - The Journal of Organic …, 2023 - ACS Publications
In this work, we developed a facile and controllable electrophilic aromatic nitration method with commercially available 68% HNO3 as the nitrating reagent and …
A Isidro‐Llobet, J Guasch‐Camell, M Álvarez… - 2005 - Wiley Online Library
Abstract p‐Nitrobenzyloxycarbonyl (pNZ) was used as a temporary protecting group for α‐ amino functionalities in solid‐phase peptide synthesis. The corresponding derivatives are …
JT Kuethe, KG Childers - Advanced Synthesis & Catalysis, 2008 - Wiley Online Library
Abstract The Suzuki–Miyaura cross‐coupling of 2‐nitrodiazonium tetrafluoroborate salts with substituted boronic acids is an effective and efficient means of preparing highly …
W Zeng, TE Ballard, AG Tkachenko, VA Burns… - Bioorganic & medicinal …, 2006 - Elsevier
Under appropriate electronic modulation, simple diazofluorene analogs recapitulate the DNA cleavage activity of kinamycin D under thiol-based reducing conditions. Achieving DNA …
MJ Sienkowska, JM Farrar, F Zhang… - Journal of Materials …, 2007 - pubs.rsc.org
A series of closely related tetrasubstituted derivatives of benzo [c] cinnoline (1), tetraazapyrene (2), phenanthrene (3), and pyrene (4) were investigated for their mesogenic …
Ferrocene catalysed C–H arylation of benzene using aryldiazonium salt is studied. Yield of biphenyl in this reaction was found to be better than some of the known methods …
G Conte, F Ely, H Gallardo - Liquid crystals, 2005 - Taylor & Francis
The design and synthesis of chiral liquid crystalline compounds based on the [1, 2, 3]‐ triazole heterocycle using the click chemistry modular approach is presented. The target …
RR González, L Liguori, AM Carrillo… - The Journal of Organic …, 2005 - ACS Publications
Mechanistic investigations and protocols for the synthesis of 2-nitrobiphenyls and 2, 2 '- dinitrobiphenyls are disclosed. It is revealed that obstacles appear during the …
JT Manka, VC McKenzie… - The Journal of Organic …, 2004 - ACS Publications
Aryldiazo substituents were used in nucleophilic aromatic substitution reactions of halogens. The Ph-N N− group activates ortho fluorine atoms toward alkylthiolation under mild …