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Covalent organic frameworks
KT Tan, S Ghosh, Z Wang, F Wen… - Nature Reviews …, 2023 - nature.com
The dream to prepare well-defined materials drives the methodological evolution for
molecular synthesis, structural control and materials manufacturing. Among various …
molecular synthesis, structural control and materials manufacturing. Among various …
Recent advances in enantioselective Pd-catalyzed allylic substitution: from design to applications
This Review compiles the evolution, mechanistic understanding, and more recent advances
in enantioselective Pd-catalyzed allylic substitution and decarboxylative and oxidative allylic …
in enantioselective Pd-catalyzed allylic substitution and decarboxylative and oxidative allylic …
Asymmetric Ni-catalyzed radical relayed reductive coupling
X Wei, W Shu, A García-Domínguez… - Journal of the …, 2020 - ACS Publications
Alkene dicarbofunctionalizations enable the streamlined construction of aliphatic structures
and have thus been the subject of intense research efforts. Despite significant progress …
and have thus been the subject of intense research efforts. Despite significant progress …
Ligand acceleration in chiral Lewis acid catalysis
S Dong, W Cao, M Pu, X Liu, X Feng - CCS Chemistry, 2023 - chinesechemsoc.org
Ligand-accelerated catalysis (LAC), a term originally coined by Sharpless, has been a
pivotal guiding principle in the advancement of asymmetric catalysis. The discovery and …
pivotal guiding principle in the advancement of asymmetric catalysis. The discovery and …
Pd/IPrBIDEA-Catalyzed Hydrodefluorination of gem-Difluorocyclopropanes: Regioselective Synthesis of Terminal Fluoroalkenes
Develo** new strategies to enable chemo-and regioselective reductions is an important
topic in chemical research. Herein, an efficient and regioselective Pd/IPrBIDEA-catalyzed …
topic in chemical research. Herein, an efficient and regioselective Pd/IPrBIDEA-catalyzed …
Electroreductive olefin–ketone coupling
A user-friendly approach is presented to sidestep the venerable Grignard addition to
unactivated ketones to access tertiary alcohols by reversing the polarity of the disconnection …
unactivated ketones to access tertiary alcohols by reversing the polarity of the disconnection …
Catalytic Chemo- and Enantioselective Transformations of gem-Diborylalkanes and (Diborylmethyl)metallic Species
Y Lee, S Han, SH Cho - Accounts of Chemical Research, 2021 - ACS Publications
Conspectus Chemo-and stereoselective transformations of polyborylalkanes are powerful
and efficient methods to access optically active molecules with greater complexity and …
and efficient methods to access optically active molecules with greater complexity and …
Palladium‐Catalyzed Cascade Heck Coupling and Allylboration of Iododiboron Compounds via Diboryl Radicals
Y Wei, XY **e, J Liu, X Liu, B Zhang… - Angewandte …, 2024 - Wiley Online Library
Geminal bis (boronates) are versatile synthetic building blocks in organic chemistry. The fact
that they predominantly serve as nucleophiles in the previous reports, however, has …
that they predominantly serve as nucleophiles in the previous reports, however, has …
gem-Diborylalkanes: recent advances in their preparation, transformation and application
Recently, gem-diborylalkanes have attracted much attention as versatile building blocks and
fundamental intermediates in organic synthesis, because they enable multiple C–C bond …
fundamental intermediates in organic synthesis, because they enable multiple C–C bond …
Ir‐Catalyzed Enantioselective Synthesis of gem‐Diborylalkenes Enabled by 1,2‐Boron Shift
JF Ge, XZ Zou, XR Liu, CL Ji, XY Zhu… - Angewandte Chemie …, 2023 - Wiley Online Library
Asymmetric cross‐couplings based on 1, 2‐carbon migration from B‐ate complexes have
been developed efficiently to access valuable organoboronates. However, enantioselective …
been developed efficiently to access valuable organoboronates. However, enantioselective …