Adding Spatial Control to Click Chemistry: Phototriggered Diels-Alder Surface (Bio)functionalization at Ambient Temperature

2011 ◽  
Vol 51 (4) ◽  
pp. 1071-1074 ◽  
Author(s):  
Thomas Pauloehrl ◽  
Guillaume Delaittre ◽  
Volker Winkler ◽  
Alexander Welle ◽  
Michael Bruns ◽  
...  
Keyword(s):  
Ambient Temperature ◽  
Click Chemistry ◽  
Diels Alder ◽  
Spatial Control

Shining Light on Cyclopentadienone–Norbornadiene Diels–Alder Adducts to Enable Photoinduced Click Chemistry with Cyclopentadiene

2021 ◽  
Author(s):  
Sophia J. Bailey ◽  
Friedrich Stricker ◽  
Erik Hopkins ◽  
Maxwell Z. Wilson ◽  
Javier Read de Alaniz
Keyword(s):  
Click Chemistry ◽  
Diels Alder

scholarly journals A click chemistry-based microRNA maturation assay optimized for high-throughput screening

2016 ◽  
Vol 52 (53) ◽  
pp. 8267-8270 ◽  
Author(s):  
Daniel A. Lorenz ◽  
Amanda L. Garner
Keyword(s):  
Click Chemistry ◽  
High Throughput ◽  
High Throughput Screening ◽  
Diels Alder ◽  
Inverse Electron Demand ◽  
Electron Demand

A catalytic enzyme-linked click chemistry assay (cat-ELCCA) for Dicer-catalyzed pre-microRNA maturation was optimized to employ inverse-electron demand Diels–Alder (IEDDA) chemistry affording high-throughput screening capability.

Self-healable Functional Polymers based on Diels-Alder ‘Click Chemistry’ Involving Substituted Furan and Triazolinedione Derivatives; A Simple and Very Fast Approach

2021 ◽  
Author(s):  
Prantik Mondal ◽  
Gourhari Jana ◽  
Tuhin Subhra Pal ◽  
Pratim K. Chattaraj ◽  
Nikhil K Singha
Keyword(s):  
Click Chemistry ◽  
Materials Science ◽  
Functional Polymers ◽  
Diels Alder ◽  
Polymer Materials ◽  
Self Healing ◽  
Natural Phenomena ◽  
Science And Engineering ◽  
Fast Approach ◽  
Materials Science And Engineering

Nowadays, the design of functional polymer materials that can mimic natural phenomena, e.g., self-healing of skin cuts, has got a tremendous interest in materials science and engineering. Recently, 1,2,4-triazoline-3,5-dione (TAD)...

An Eco-Friendly Scheme for the Cross-Linked Polybutadiene Elastomer via Thiol–Ene and Diels–Alder Click Chemistry

2015 ◽  
Vol 48 (11) ◽  
pp. 3539-3546 ◽  
Author(s):  
Jing Bai ◽  
Hui Li ◽  
Zixing Shi ◽  
Jie Yin
Keyword(s):  
Click Chemistry ◽  
Diels Alder ◽  
The Cross

Retro aza Diels-Alder reactions: acid catalyzed heterocycloreversion of 2-azanorbornenes in water at ambient temperature

1987 ◽  
Vol 109 (19) ◽  
pp. 5859-5861 ◽  
Author(s):  
Paul A. Grieco ◽  
David T. Parker ◽  
Michael Cornwell ◽  
Robert Ruckle
Keyword(s):  
Ambient Temperature ◽  
Diels Alder ◽  
Acid Catalyzed

scholarly journals Correction: An injectable hyaluronic acid/PEG hydrogel for cartilage tissue engineering formed by integrating enzymatic crosslinking and Diels–Alder “click chemistry”

2018 ◽  
Vol 9 (28) ◽  
pp. 3959-3960 ◽  
Author(s):  
Feng Yu ◽  
Xiaodong Cao ◽  
Yuli Li ◽  
Lei Zeng ◽  
Bo Yuan ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Hyaluronic Acid ◽  
Click Chemistry ◽  
Cartilage Tissue Engineering ◽  
Diels Alder ◽  
Cartilage Tissue

Correction for ‘An injectable hyaluronic acid/PEG hydrogel for cartilage tissue engineering formed by integrating enzymatic crosslinking and Diels–Alder “click chemistry”’ by Feng Yu et al., Polym. Chem., 2014, 5, 1082–1090.

Improving excretory pathways of technetium-99m SPECT imaging agents based on bioorthogonal Diels-Alder click chemistry

2019 ◽  
Vol 72-73 ◽  
pp. S65
Author(s):  
J. Walsh ◽  
L. Francesconi ◽  
V. Sanders ◽  
D. Iskhakov ◽  
B. Zeglis ◽  
...  
Keyword(s):  
Click Chemistry ◽  
Diels Alder ◽  
Spect Imaging ◽  
Imaging Agents ◽  
Technetium 99M

scholarly journals A mutually stabilized host-guest pair

2019 ◽  
Vol 5 (11) ◽  
pp. eaax6707 ◽  
Author(s):  
Chi Zhang ◽  
Hongye Wang ◽  
Jie Zhong ◽  
Ye Lei ◽  
Renfeng Du ◽  
...  
Keyword(s):  
Click Chemistry ◽  
Uv Light ◽  
Alder Reaction ◽  
Diels Alder ◽  
Protecting Group ◽  
Face To Face ◽  
Π Interactions ◽  
Diels Alder Reaction

By using click chemistry, a hexacationic cage was synthesized. The cage contains two triscationic π-electron–deficient trispyridiniumtriazine (TPZ3+) platforms that are bridged in a face-to-face manner by three ethylene-triazole-ethylene linkers. A diversity of π-electron–rich guests can be recognized within the pocket of the cage, driven by host-guest π-π interactions. The cage cavity acts as a protecting group, preventing an anthracene guest from undergoing Diels-Alder reaction. Under ultraviolet (UV) light, the pyridinium C─N bonds in TPZ3+ platforms are polarized and weakened, resulting in the occurrence of cage decomposition via β-elimination. Guest recognition could help to prevent this UV-stimulated cage decomposition by suppressing the excitation of the TPZ3+ units.

scholarly journals Extension of the PNA world by functionalized PNA monomers eligible candidates for inverse Diels Alder Click Chemistry

2010 ◽  
pp. 213-223 ◽  
Author(s):  
Manfred Wiessler ◽  
Waldemar Waldeck ◽  
Ruediger Pipkorn ◽  
Christian Kliem ◽  
Peter Lorenz ◽  
...  
Keyword(s):  
Click Chemistry ◽  
Diels Alder
Sign in / Sign up

Export Citation Format

Share Document