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BIOTAGE endeavor catalyst screening system
Endeavor Catalyst Screening System, supplied by BIOTAGE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/catalyst+screening/endeavor+catalyst+screening+system/pm34652911-249-8-7
Average 90 stars, based on 1 article reviews
endeavor catalyst screening system - by Bioz Stars, 2026-10
90/100 stars

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Article Title: Preparation of monocarbonyl ruthenium complexes bearing bidentate nitrogen and phosphine ligands and their catalytic activity in carbonyl compound reduction.
Article Snippet: The monocarbonyl complexes [RuCl2(CO)(PR3)(NN)] (R = Cy, NN = en 1, ampy 2; R = iPr; NN = en 3) have been prepared in a one pot reaction from [RuCl2(CO)(dmf)(PPh3)2], PR3 and the NN ligand in CH2Cl2.. Treatment of the [Ru(OAc)2(CO)(PPh3)2] with NN ligands in methanol gives the cationic derivatives [Ru(OAc)(CO)(PPh3)(NN)]OAc (NN = en 4, ampy 5) in which one acetate acts as bidentate ligand, whereas the other is not coordinated.. The diphosphine complexes [RuCl2(CO)(PP)(PPh3)] (PP = dppb 6, dppf 7, (R)-BINAP 8, (R,Sp)-Josiphos 9 and (R,R)-Skewphos 10) have been obtained starting from [RuCl2(CO)(dmf)(PPh3)2] and the PP ligand in CHCl3 or toluene at reflux.

Article Title: Preparation of Neutral trans - cis [Ru(O2CR)2P2(NN)], Cationic [Ru(O2CR)P2(NN)](O2CR) and Pincer [Ru(O2CR)(CNN)P2] (P = PPh3, P2 = diphosphine) Carboxylate Complexes and their Application in the Catalytic Carbonyl Compounds Reduction
Article Snippet: The HY reactions were performed in an eight-vessel Endeavor Biotage apparatus.

Article Title: Understanding catalytic hydrogenolysis of 5-hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) using carbon supported Ru catalysts
Article Snippet: Herein, our study has demonstrated that microporous carbon supported Ru catalysts can selectively convert 5hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) in isopropanol through hydrogenolysis in a catalytic ratio of 2.47mol% under 5 bar of hydrogen at 125 °C for 1 h. DMF yield can reach 69.52% with complete HMF conversion.. The effects of reaction temperature, hydrogen pressure, metal loading and reaction solvent for hydrogenolysis have been carefully investigated.. In addition, to better understand the influence of the intrinsic nature of carbonaceous material, carbon materials possessing different surface texture including microporosity, mesoporosity and nonporous carbon black were used as catalyst supports, and structural properties have been comprehensively characterized by powder X-ray diffraction spectrometer (PXRD), transmission electron microscopy (TEM), nitrogen and CO2 sorption, thermogravimetric analysis (TGA), and X-ray absorption spectroscopy (XAS).

Article Title: Preparation of Neutral trans - cis [Ru(O2CR)2P2(NN)], Cationic [Ru(O2CR)P2(NN)](O2CR) and Pincer [Ru(O2CR)(CNN)P2] (P = PPh3, P2 = diphosphine) Carboxylate Complexes and their Application in the Catalytic Carbonyl Compounds Reduction
Article Snippet: The HY reactions have been carried out in a catalyst screening system (eight-vessels Endeavor Biotage system), which allows parallel reactions to be followed.

Article Title: Using the Colloidal Method to Prepare Au Catalysts for the Alkylation of Aniline by Benzyl Alcohol
Article Snippet: An Endeavor ® catalyst screening system (Biotage) was employed in this part of the work.

Article Title: Using the Colloidal Method to Prepare Au Catalysts for the Alkylation of Aniline by Benzyl Alcohol.
Article Snippet: An Endeavor® catalyst screening system (Biotage) was employed in this part of the work.

Article Title: Exploration of a Nitromethane-Carbonylation Strategy during Route Design of an Atropisomeric KRAS G12C Inhibitor.
Article Snippet: Route design and proof of concept synthesis was conducted on a synthetically challenging atropisomeric KRAS inhibitor to support clinical API manufacture.. Improvements to the synthesis of a chiral piperazine fragment gave reduced step count and streamlined protecting group strategy via the formation and methanol ring opening of an N-carboxy-anhydride (NCA).. The complex atropisomeric nitroquinoline was accessed via an early stage salt-resolution followed by a formal two-part nitromethanecarbonylation, avoiding a high temperature Gould−Jacobs cyclization that previously led to atropisomer racemization.

Article Title: Productive Homogeneous Hydrogenation of Fatty Esters with Carboxylate SNS Ruthenium Catalysts.
Article Snippet: Typical procedure for HY of methyl and ethyl esters The HY reductions of a series of methyl and ethyl esters were performed in an 8 vessels Endeavor Biotage apparatus employing the catalysts 1, 2 and trans-[RuCl2(SNS)(PPh3)], following the procedure used for methyl decanoate.



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