Results 251 to 260 of about 6,058,834 (370)

Design of Waveguide NbN‐Based Superconductor–Insulator–Superconductor Mixer for 650 GHz

open access: yesAdvanced Photonics Research, EarlyView.
This research work focuses on a waveguide NbN‐based superconductor–insulator–superconductor mixer operating at 650 GHz. The signal coupling circuit is designed using a waveguide‐microstrip coupling structure, and the return loss obtained is lower than −16 dB. For the mixing circuit, its return loss is less than −7.5 dB, and the return loss reduces with
Lianhao He, Fangting Lin, Xiaoyong He
wiley   +1 more source

Effective and Practical Stereoselective Synthesis of Nutlins Precursors by Immobilization of Privileged Chiral Mono‐Amidine Catalyst

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
Abstract A strategy for the immobilization of Johnston's Mono(AMidine) catalyst (MAM) onto polystyrene, silica and hybrid silica‐polystyrene nanoparticles is presented. The catalyst activity was evaluated in the stereoselective aza‐Henry reaction leading to the pivotal β‐amino nitroalkane precursors of the anti‐cancer agents Nutlins (with Nutlin‐3a as ...
Sofia Toldo   +8 more
wiley   +1 more source

Ten years of change: National Library of Medicine TOXMAP gets a new look. [PDF]

open access: yesMed Ref Serv Q, 2014
Hochstein C, Gemoets D, Goshorn J.
europepmc   +1 more source

Development of Photo‐Biocatalytic Redox System for Asymmetric Synthesis of Optically Active Amines Using Blue Light and Transaminases. A Case Study Toward Mavacamten

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
Abstract α‐Chiral amines are versatile building blocks for the asymmetric synthesis of optically pure high‐added‐value chemicals, including pharmaceuticals, agrochemicals, and natural products. Herein, we report a one‐pot, two‐step sequential deracemization of racemic sec‐alcohols to optically enriched primary amines throught a photo‐biocatalytic ...
Natalia Antos   +5 more
wiley   +1 more source

Development of Hydrofluoroolefin (HFO)‐based direct O‐fluoroalkenylation of phenols targeting tyrosine conjugation

open access: yesAdvanced Synthesis &Catalysis, Accepted Article.
Methodology for direct fluoroalkenylation of phenolic OH function was developed using a fluorinated electrophilic reagent derived from HFO1234ze gas. Besides various functionalized phenols, tyrosine and tyrosine‐based peptides were successfully conjugated under the optimized reaction conditions.
Rihárd Sisa   +2 more
wiley   +1 more source

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