Progress in organocatalysis with hypervalent iodine catalysts
FV Singh, SE Shetgaonkar, M Krishnan… - Chemical Society …, 2022 - pubs.rsc.org
Hypervalent iodine compounds as environmentally friendly and relatively inexpensive
reagents have properties similar to transition metals. They are employed as alternatives to …
reagents have properties similar to transition metals. They are employed as alternatives to …
Advances in synthetic applications of hypervalent iodine compounds
A Yoshimura, VV Zhdankin - Chemical reviews, 2016 - ACS Publications
The preparation, structure, and chemistry of hypervalent iodine compounds are reviewed
with emphasis on their synthetic application. Compounds of iodine possess reactivity similar …
with emphasis on their synthetic application. Compounds of iodine possess reactivity similar …
Organocatalysis in inert C–H bond functionalization
Y Qin, L Zhu, S Luo - Chemical reviews, 2017 - ACS Publications
As two coexisting and fast-growing research fields in modern synthetic chemistry, the
merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint …
merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint …
Enroute sustainability: metal free C–H bond functionalisation
The term “C–H functionalisation” incorporates C–H activation followed by its transformation.
In a single line, this can be defined as the conversion of carbon–hydrogen bonds into …
In a single line, this can be defined as the conversion of carbon–hydrogen bonds into …
Triiodide‐Mediated δ‐Amination of Secondary C− H Bonds
EA Wappes, SC Fosu, TC Chopko… - Angewandte …, 2016 - Wiley Online Library
The Cδ− H amination of unactivated, secondary C− H bonds to form a broad range of
functionalized pyrrolidines has been developed by a triiodide (I3−)‐mediated strategy. By in …
functionalized pyrrolidines has been developed by a triiodide (I3−)‐mediated strategy. By in …
Collective approach to advancing C–H functionalization
HML Davies, D Morton - ACS Central Science, 2017 - ACS Publications
C–H functionalization is a very active research field that has attracted the interest of
scientists from many disciplines. This Outlook describes the collaborative efforts within the …
scientists from many disciplines. This Outlook describes the collaborative efforts within the …
Electrochemical Formation of N-Acyloxy Amidyl Radicals and Their Application: Regioselective Intramolecular Amination of sp2 and sp3 C–H Bonds
S Zhang, L Li, M Xue, R Zhang, K Xu, C Zeng - Organic letters, 2018 - ACS Publications
Electrochemical generation of N-acyloxy amidyl radicals via an inner-sphere electron-
transfer process is described for the first time. With NaBr as the catalyst and electrolyte, the …
transfer process is described for the first time. With NaBr as the catalyst and electrolyte, the …
Visible‐Light‐Catalyzed Direct Benzylic C(sp3)–H Amination Reaction by Cross‐Dehydrogenative Coupling
A conceptually new and synthetically valuable cross‐dehydrogenative benzylic C (sp3)–H
amination reaction is reported by visible‐light photoredox catalysis. This protocol employs …
amination reaction is reported by visible‐light photoredox catalysis. This protocol employs …
C–F bond cleavage enabled redox-neutral [4+ 1] annulation via C–H bond activation
CQ Wang, L Ye, C Feng, TP Loh - Journal of the American …, 2017 - ACS Publications
Using α, α-difluoromethylene alkyne as a nontraditional one-carbon reaction partner, a
synthetically novel method for the construction of isoindolin-1-one derivatives via Rh (III) …
synthetically novel method for the construction of isoindolin-1-one derivatives via Rh (III) …
Organocatalytic electrochemical amination of benzylic C–H bonds
ZW Hou, L Li, L Wang - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
An organocatalytic site-selective electrochemical method for the benzylic C–H amination
reactions of alkylarenes with azoles through hydrogen evolution has been developed. The …
reactions of alkylarenes with azoles through hydrogen evolution has been developed. The …