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 …
Sequential and direct multicomponent reaction (MCR)-based dearomatization strategies
Dearomatization strategies in a multicomponent fashion often result in complex heterocyclic
frameworks, which have attracted the attention of chemists due to their natural product-like …
frameworks, which have attracted the attention of chemists due to their natural product-like …
Photoredox-enabled dearomative [2π+ 2σ] cycloaddition of phenols
S Dutta, D Lee, K Ozols, CG Daniliuc… - Journal of the …, 2024 - ACS Publications
Dearomative photocycloaddition of monocyclic arenes is an appealing strategy for
comprehending the concept of “escape from flatland”. This brings the replacement of readily …
comprehending the concept of “escape from flatland”. This brings the replacement of readily …
Chiral hypervalent iodines: active players in asymmetric synthesis
A Parra - Chemical reviews, 2019 - ACS Publications
Asymmetric organocatalytic oxidations have been witnessed to an impressive development
in the last years thanks to the establishment of important chiral hypervalent iodines (III/V) …
in the last years thanks to the establishment of important chiral hypervalent iodines (III/V) …
Chemistry of polyvalent iodine
VV Zhdankin, PJ Stang - Chemical reviews, 2008 - ACS Publications
Starting from the early 1990s, the chemistry of polyvalent iodine organic compounds has
experienced an explosive development. This surging interest in iodine compounds is mainly …
experienced an explosive development. This surging interest in iodine compounds is mainly …
Asymmetric Dearomatization of Naphthols via a Rh-Catalyzed C(sp2)–H Functionalization/Annulation Reaction
J Zheng, SB Wang, C Zheng… - Journal of the American …, 2015 - ACS Publications
A Rh-catalyzed enantioselective dearomatization of 1-aryl-2-naphthols with internal alkynes
via C–H functionalization reaction was achieved. In the presence of a chiral Cp/Rh catalyst …
via C–H functionalization reaction was achieved. In the presence of a chiral Cp/Rh catalyst …
meta-Selective C–H arylation of phenols via regiodiversion of electrophilic aromatic substitution
A Senior, K Ruffell, LT Ball - Nature Chemistry, 2023 - nature.com
Electrophilic aromatic substitution is among the most widely used mechanistic manifolds in
organic chemistry. Access to certain substitution patterns is, however, precluded by intrinsic …
organic chemistry. Access to certain substitution patterns is, however, precluded by intrinsic …
Enantioselective Kita oxidative spirolactonization catalyzed by in situ generated chiral hypervalent iodine (III) species
M Uyanik, T Yasui, K Ishihara - Angewandte Chemie International Edition, 2010 - infona.pl
The iodines (III) have it: The rational design of a conformationally flexible C 2‐symmetric
iodosylarene catalyst has been used for the enantioselective Kita oxidative …
iodosylarene catalyst has been used for the enantioselective Kita oxidative …
Cooperative catalysis of Co single atoms and nanoparticles enables selective CAr− OCH3 cleavage for sustainable production of lignin-based cyclohexanols
In this work, a dual-size MOF-derived Co catalyst (0.2 Co 1-NPs@ NC) composed of single
atoms (Co 1) and highly dispersed nanoparticles (Co NPs) was prepared by in-situ Zn …
atoms (Co 1) and highly dispersed nanoparticles (Co NPs) was prepared by in-situ Zn …
Asymmetric dearomatizing spirolactonization of naphthols catalyzed by spirobiindane-based chiral hypervalent iodine species
T Dohi, N Takenaga, T Nakae, Y Toyoda… - Journal of the …, 2013 - ACS Publications
This report details the development of a spirobiindane-based chiral hypervalent iodine
reagent, especially focusing on its structural elucidation for effective asymmetric induction of …
reagent, especially focusing on its structural elucidation for effective asymmetric induction of …