Phosphine organocatalysis
The hallmark of nucleophilic phosphine catalysis is the initial nucleophilic addition of a
phosphine to an electrophilic starting material, producing a reactive zwitterionic …
phosphine to an electrophilic starting material, producing a reactive zwitterionic …
Phosphine-catalyzed asymmetric organic reactions
Asymmetric phosphine catalysis showcasing remarkable progress over the past two
decades has emerged as a key synthetic platform for the creation of molecular frameworks …
decades has emerged as a key synthetic platform for the creation of molecular frameworks …
Synthesis of heterocyclic compounds through nucleophilic phosphine catalysis
Y Huang, J Liao, W Wang, H Liu, H Guo - Chemical Communications, 2020 - pubs.rsc.org
Nucleophilic phosphine catalysis is a practical and powerful tool for the synthesis of various
heterocyclic compounds with the advantages of environmentally friendly, metal-free, and …
heterocyclic compounds with the advantages of environmentally friendly, metal-free, and …
Phosphine‐catalyzed enantioselective dearomative [3+ 2]‐cycloaddition of 3‐nitroindoles and 2‐nitrobenzofurans
H Wang, J Zhang, Y Tu, J Zhang - Angewandte Chemie, 2019 - Wiley Online Library
Over the past years, the metal‐catalyzed dearomative cycloaddition of 3‐nitroindoles and 2‐
nitrobenzofurans have emerged as a powerful protocol to construct chiral fused heterocyclic …
nitrobenzofurans have emerged as a powerful protocol to construct chiral fused heterocyclic …
Chiral monophosphorus ligands for asymmetric catalytic reactions
Chiral monophosphorus ligands are playing an important role for the recent advances in
asymmetric catalysis. This review summarizes the latest progress in various asymmetric …
asymmetric catalysis. This review summarizes the latest progress in various asymmetric …
Crystallography of encapsulated molecules
K Rissanen - Chemical Society Reviews, 2017 - pubs.rsc.org
The crystallography of supramolecular host–guest complexes is reviewed and discussed as
a part of small molecule crystallography. In these complexes, the host binds the guests …
a part of small molecule crystallography. In these complexes, the host binds the guests …
Asymmetric Synthesis of Spirocyclic β‐Lactams through Copper‐Catalyzed Kinugasa/Michael Domino Reactions
T Shu, L Zhao, S Li, XY Chen… - Angewandte Chemie …, 2018 - Wiley Online Library
The first copper‐catalyzed highly chemo‐, regio‐, diastereo‐, and enantioselective
Kinugasa/Michael domino reaction for the desymmetrization of prochiral cyclohexadienones …
Kinugasa/Michael domino reaction for the desymmetrization of prochiral cyclohexadienones …
Enantioselective Catalysis by the Umpolung of Conjugate Acceptors Involving N-Heterocyclic Carbene or Organophosphine 1, 4-Addition
Y Nakano, JT Maddigan-Wyatt… - Accounts of Chemical …, 2023 - ACS Publications
Conspectus Conjugate acceptors are one of the most common electrophilic functional
groups in organic synthesis. While useful in a diverse range of transformations, their …
groups in organic synthesis. While useful in a diverse range of transformations, their …
Exploration of flow reaction conditions using machine-learning for enantioselective organocatalyzed Rauhut–Currier and [3+ 2] annulation sequence
M Kondo, HDP Wathsala, M Sako, Y Hanatani… - Chemical …, 2020 - pubs.rsc.org
A highly atom-economical enantioselective organocatalyzed Rauhut–Currier and [3+ 2]
annulation sequence has been established by using a flow system. Suitable flow conditions …
annulation sequence has been established by using a flow system. Suitable flow conditions …
Stereocontrolled transformations of cyclohexadienone derivatives to access stereochemically rich and natural product-inspired architectures
The last two decades or so have witnessed an upsurge in defining the art of designing
complex natural products and nature-inspired molecules. Throughout these decades …
complex natural products and nature-inspired molecules. Throughout these decades …