Concerted reactions that produce diradicals and zwitterions: electronic, steric, conformational, and kinetic control of cycloaromatization processes
RK Mohamed, PW Peterson, IV Alabugin - Chemical Reviews, 2013 - ACS Publications
The broad utility of cyclic structures accounts for the key roles that cycle-forming reactions
play in synthetic designs. Most of these reactions can be classified as either a cyclization of …
play in synthetic designs. Most of these reactions can be classified as either a cyclization of …
Design, synthesis, and biological activity of unnatural enediynes and related analogues equipped with pH-dependent or phototriggering devices
M Kar, A Basak - Chemical reviews, 2007 - ACS Publications
Design, Synthesis, and Biological Activity of Unnatural Enediynes and Related Analogues
Equipped with pH-Dependent or Phototriggering Devices | Chemical Reviews ACS ACS …
Equipped with pH-Dependent or Phototriggering Devices | Chemical Reviews ACS ACS …
Fluorescent “light-up” bioprobes based on tetraphenylethylene derivatives with aggregation-induced emission characteristics
H Tong, Y Hong, Y Dong, M Häußler… - Chemical …, 2006 - pubs.rsc.org
Fluorescent “light-up” bioprobes based on tetraphenylethylene derivatives with aggregation-induced
emission characteristics - Chemical Communications (RSC Publishing) DOI:10.1039/B608425G …
emission characteristics - Chemical Communications (RSC Publishing) DOI:10.1039/B608425G …
Hybrids of amino acids and acetylenic DNA-photocleavers: optimising efficiency and selectivity for cancer phototherapy
Hybrid agents which combine potent DNA-photocleavers with tunable amino acids or small
peptides were designed to improve selectivity of Nature's most potent class of antibiotics …
peptides were designed to improve selectivity of Nature's most potent class of antibiotics …
A novel enediynyl peptide inhibitor of furin that blocks processing of proPDGF-A, B and proVEGF-C
Background Furin represents a crucial member of secretory mammalian subtilase, the
Proprotein Convertase (PC) or Proprotein Convertase Subtilisin/Kexin (PCSK) superfamily. It …
Proprotein Convertase (PC) or Proprotein Convertase Subtilisin/Kexin (PCSK) superfamily. It …
A Strategy for Dramatically Enhancing the Selectivity of Molecules Showing Aggregation‐Induced Emission towards Biomacromolecules with the Aid of Graphene …
X Xu, J Li, Q Li, J Huang, Y Dong… - … A European Journal, 2012 - Wiley Online Library
By intelligently utilizing the different interacting strengths between different moieties
according to the displacement method, general biosensors with aggregation‐induced …
according to the displacement method, general biosensors with aggregation‐induced …
Folate-conjugated gold nanoparticles (synthesis, characterization and design for cancer cells nanotechnology-based targeting)
A new folate-conjugated gold nanoparticle (AuNP) has been designed to selectively target
the folate receptor that is overexpressed on the surface of tumoral cells. For this purpose, we …
the folate receptor that is overexpressed on the surface of tumoral cells. For this purpose, we …
Synthesis of Novel “Rod− Coil” Brush Polymers with Conjugated Backbones through Bergman Cyclization
X Cheng, J Ma, J Zhi, X Yang, A Hu - Macromolecules, 2010 - ACS Publications
This work reports synthesis of “rod− coil” brush polymers with rigid conjugated
backbone.“Grafting through” strategy was employed via combination of ring-opening …
backbone.“Grafting through” strategy was employed via combination of ring-opening …
Triazolo-β-aza-ε-amino acid and its aromatic analogue as novel scaffolds for β-turn peptidomimetics
Triazolo-β-aza-ε-amino acid and its aromatic analogue (AlTAA/ArTAA) in the peptide
backbone mark a novel class of conformationally constrained molecular scaffolds to induce …
backbone mark a novel class of conformationally constrained molecular scaffolds to induce …
Syntheses and antibacterial activity of phendioxy substituted cyclic enediynes
MC Joshi, GS Bisht, DS Rawat - Bioorganic & medicinal chemistry letters, 2007 - Elsevier
Syntheses and antibacterial activity of phendioxy substituted cyclic enediynes - ScienceDirect
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