Visible-to-NIR-light activated release: from small molecules to nanomaterials

R Weinstain, T Slanina, D Kand, P Klan - Chemical reviews, 2020 - ACS Publications
Photoactivatable (alternatively, photoremovable, photoreleasable, or photocleavable)
protecting groups (PPGs), also known as caged or photocaged compounds, are used to …

Photoremovable protecting groups in chemistry and biology: reaction mechanisms and efficacy

P Klán, T Solomek, CG Bochet, A Blanc… - Chemical …, 2013 - ACS Publications
Photoremovable Protecting Groups in Chemistry and Biology: Reaction Mechanisms and
Efficacy | Chemical Reviews ACS ACS Publications C&EN CAS Find my institution Log In …

[图书][B] Photochemistry of organic compounds: from concepts to practice

P Klán, J Wirz - 2009 - books.google.com
Photochemistry of Organic Compounds: From Concepts to Practice provides a hands-on
guide demonstrating the underlying principles of photochemistry and, by reference to a …

Photolabile protecting groups and linkers

CG Bochet - Journal of the Chemical Society, Perkin Transactions 1, 2002 - pubs.rsc.org
Protecting groups are a painful necessity in organic synthesis, despite all the drawbacks
associated with their use. 1–3 Indeed, in addition to the fact that their introduction and …

[图书][B] CRC Handbook of Organic Photochemistry and Photobiology, Volumes 1 & 2

WM Horspool, F Lenci - 2003 - taylorfrancis.com
The second edition of this best-selling handbook is bigger, more comprehensive, and now
completely current. In addition to thorough updates to the discussions featured in the first …

Photolabile protecting groups: structure and reactivity

P Wang - Asian Journal of Organic Chemistry, 2013 - Wiley Online Library
This Review focuses on the structure‐reactivity relationship of three main classes of
photolabile protecting groups (PPGs), that is, the 2‐nitrobenzyl (NB) series of PPGs …

New Phototriggers 9:  p-Hydroxyphenacyl as a C-Terminal Photoremovable Protecting Group for Oligopeptides

RS Givens, JFW Weber, PG Conrad… - Journal of the …, 2000 - ACS Publications
In our search for a more versatile protecting group that would exhibit fast release rates for
peptides, we have designed and developed the p-hydroxyphenacyl (pHP) group as a new …

Radical biocatalysis: Using non-natural single electron transfer mechanisms to access new enzymatic functions

TK Hyster - Synlett, 2020 - thieme-connect.com
Exploiting non-natural reaction mechanisms within native enzymes is an emerging strategy
for expanding the synthetic capabilities of biocatalysts. When coupled with modern protein …

Photoactivatable fluorescent probes for spatiotemporal-controlled biosensing and imaging

Z Zou, Z Luo, X Xu, S Yang, Z Qing, J Liu… - TrAC Trends in Analytical …, 2020 - Elsevier
Designing fluorescent probes for accurately analyzing target molecules of interest become
fascinating and vital in the view of biology and biomedicine. Conventional fluorescent …

Electrosynthesis of enaminones directly from methyl ketones and amines with nitromethane as a carbon source

K Xu, Z Zhang, P Qian, Z Zha, Z Wang - Chemical Communications, 2015 - pubs.rsc.org
An efficient and mechanistically different method for the electrosynthesis of enaminone
directly from methyl ketones, amines and nitromethane was developed. This transition-metal …