Asymmetric catalytic rearrangements with α-diazocarbonyl compounds
S Dong, X Liu, X Feng - Accounts of Chemical Research, 2022 - ACS Publications
Conspectus α-Diazocarbonyl compounds serve as nucleophiles, dipoles, carbene
precursors, and rare electrophiles, enabling a vast array of organic transformations under …
precursors, and rare electrophiles, enabling a vast array of organic transformations under …
Progress in the Synthesis and Transformations of Alkylidenecyclopropanes and Alkylidenecyclobutanes
Methylene-and alkylidenecyclopropanes (MCPs and ACPs, 1, Figure 1) and-cyclobutanes
(MCBs and ACBs, 2, Figure 1) are highly strained molecules, but at the same time most of …
(MCBs and ACBs, 2, Figure 1) are highly strained molecules, but at the same time most of …
Feng chiral N, N′-dioxide ligands: uniqueness and impacts
DF Chen, LZ Gong - Organic Chemistry Frontiers, 2023 - pubs.rsc.org
From the historical perspective, all widely accepted privileged chiral ligands tune the
catalytic activity of the metal complexes that they form and impart stereoselectivity to …
catalytic activity of the metal complexes that they form and impart stereoselectivity to …
Sequential visible-light photoactivation and palladium catalysis enabling enantioselective [4+ 2] cycloadditions
MM Li, Y Wei, J Liu, HW Chen, LQ Lu… - Journal of the American …, 2017 - ACS Publications
Catalytic asymmetric cycloadditions of reactive ketene intermediates provide new
opportunities for the production of chiral heterocyclic molecules. Though known for over 100 …
opportunities for the production of chiral heterocyclic molecules. Though known for over 100 …
A Conjugated Covalent Template Strategy for All‐Benzene Catenane Synthesis
A Bu, Y Zhao, H Xiao, CH Tung, LZ Wu… - Angewandte …, 2022 - Wiley Online Library
Mechanically interlocked molecules based on oligoparaphenylene‐derived nanohoops,
particularly those without heteroatoms, are synthetically challenging and topologically …
particularly those without heteroatoms, are synthetically challenging and topologically …
Catalytic asymmetric homologation of ketones with α-alkyl α-diazo esters
F Tan, M Pu, J He, J Li, J Yang, S Dong… - Journal of the …, 2021 - ACS Publications
The homologation of ketones with diazo compounds is a useful strategy to synthesize one-
carbon chain-extended acyclic ketones or ring-expanded cyclic ketones. However, the …
carbon chain-extended acyclic ketones or ring-expanded cyclic ketones. However, the …
Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium (III)-complex catalyzed inverse-electron-demand hetero-Diels–Alder reaction
An asymmetric inverse-electron-demand hetero-Diels–Alder reaction between o-quinone
methides and azlactones to generate potentially pharmacological active dihydrocoumarins …
methides and azlactones to generate potentially pharmacological active dihydrocoumarins …
Modern Trends of Organic Chemistry in Russian Universities
AI Konovalov, IS Antipin, VA Burilov… - Russian Journal of …, 2018 - Springer
This review is devoted to the scientific achievements of the departments of organic chemistry
in higher schools of Russia within the past decade.
in higher schools of Russia within the past decade.
Diversity-oriented approaches to unusual α-amino acids and peptides: step economy, atom economy, redox economy, and beyond
Here we describe several useful strategies to a variety of unusual α-amino acid derivatives
and peptides based on “building block” approach. These building blocks are suitable for …
and peptides based on “building block” approach. These building blocks are suitable for …
Recent advances in the synthesis of benzimidazol (on) es via rearrangements of quinoxalin (on) es
VA Mamedov - RSC advances, 2016 - pubs.rsc.org
This is the first review describing all the quinoxaline–benzimidazole rearrangements as a
whole and the new quinoxalinone–benzimidazol (on) e rearrangements in particular when …
whole and the new quinoxalinone–benzimidazol (on) e rearrangements in particular when …