Results 211 to 220 of about 143,165 (330)

Synthesis, Optical and Singlet Oxygen Generation Properties of Phenazinone‐Based Photosensitizer with 5‐Formyl‐2‐Thienyl Substituents

open access: yesAsian Journal of Organic Chemistry, EarlyView.
Phenazinone chromophore incorporating a carbonyl group into the skeleton is recently found to be a new‐type halogen‐atom‐free‐photosensitizer possessing superior ability in singlet oxygen (1O2) generation. In this work, we have designed and developed the derivative with two 5‐formyl‐2‐thienyl substituents which is expected to lead to improvement of the
Hiroto Tsuyama   +2 more
wiley   +1 more source

Insights into the Sources, Structure, and Action Mechanisms of Quinones on Diabetes: A Review. [PDF]

open access: yesMolecules
Zhang T   +6 more
europepmc   +1 more source

Synthesis of a Molecular Tweezer Based on Norbornadiene Framework: Unexpected Stereoselectivity

open access: yesAsian Journal of Organic Chemistry, EarlyView.
A new type of Klarner's molecular tweezer was synthesized through annulation of an α‐amino ketone. Surprisingly, the reaction takes place stereoselectivity though the initial amino ketone is racemic. This tweezer comprises two near‐parallel flat aromatic rings as pincers, each bearing two methyl ester groups, and a pyrazine unit as the tether ...
Evren Cücü   +3 more
wiley   +1 more source

Design Strategies Based on Electronic Interactions for Effective Catalysts in Lithium–Sulfur Batteries

open access: yesAngewandte Chemie, EarlyView.
Design of effective bidirectional electrocatalyst focused on electronic interactions in lithium–sulfur batteries. Development of effective bidirectional catalyst is essential for high‐energy density and long‐life lithium–sulfur batteries. The catalytic activity of catalyst is directly related to the degree of the interaction between the catalysts and ...
Donghyeok Son   +5 more
wiley   +2 more sources

Enantiopure Chiral Crystals: A Powerful Tool for Absolute Asymmetric Synthesis

open access: yesAsian Journal of Organic Chemistry, EarlyView.
This review covers absolute asymmetric syntheses, which allow the preparation of enantiomerically enriched chiral compounds from achiral precursors. By exploiting the crystallization of certain compounds as a conglomerate, enantiopure chiral crystals are spontaneously obtained.
Jiacheng Li, Valérie Alezra
wiley   +1 more source

Pyrazine‐Embedded 2D Conjugated Metal–Organic Framework with Quasi‐Honeycomb Lattice for High‐Capacitance Lithium‐Ion Storage

open access: yesAngewandte Chemie, EarlyView.
A Cu‐OHDDQP 2D conjugated metal–organic framework (2D c‐MOF) was synthesized possessing a unique quasi‐honeycomb topology, from a pyrazine‐fused, D2‐symmetric ligand. The achieved 2D c‐MOF electrode displayed a remarkable gravimetric capacitance up to 452 A g−1 for electrochemical lithium storage.
Xiangyu Li   +13 more
wiley   +2 more sources

Synthesis of Thiacalix[4]arene Skeleton by the Conjugate Addition of Benzoquinone. [PDF]

open access: yesJ Org Chem
Mamleev K   +6 more
europepmc   +1 more source

Diglycerides of Natural Phenols and Organic Acids for Enhanced Biological Activities

open access: yesAsian Journal of Organic Chemistry, EarlyView.
Diglycerides of natural organic acids and phenols were synthesized regio‐selectively. Diglycerides are structurally similar to cell membranes and are expected to exhibit cell affinity and permeability. The flexible glycerol linkers allow the diglycerides to exhibit not only the physiological activities of each constituent organic acid but also the ...
Jisu Hong   +10 more
wiley   +1 more source

Manganese‐Catalyzed Enantioselective Dearomative Epoxidation of Naphthalenes with Aqueous Hydrogen Peroxide

open access: yesAngewandte Chemie, EarlyView.
The enantioselective epoxidation of naphthalenes into their corresponding arene oxides with aqueous hydrogen peroxide is described. The reaction combines dearomatization with installation of chemically versatile functionality in an enantioselective manner.
Najoua Choukairi Afailal   +2 more
wiley   +2 more sources

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