المؤلفون: Qingyun Tang, Mark Petchey, Benjamin Rowlinson, Thomas J. Burden, Ian J. S. Fairlamb, Gideon Grogan

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Pharmacology, Biotechnology, Chemical Sciences not elsewhere classified, subsequent amidation using, revealing key roles, ray crystallographic structure, permitted mutational mapping, frequently performed reactions, form amine products, amine binding sites, amide bond synthetases, previously studied abs, amine coupling partners, contemporary pharmaceutical synthesis, carboxylic acid substrates, amine substrates, carboxylic acid, coupling agents, amine partner, amine nucleophile, amide bonds, pharmaceutical synthesis, activated substrates, racemic acid, chiral acid, streptoalloteichus hindustanus, stoichiometric quantities

Relation: https://figshare.com/articles/journal_contribution/Broad_Spectrum_Enantioselective_Amide_Bond_Synthetase_from_Streptoalloteichus_hindustanus/24953739

الاتاحة: https://doi.org/10.1021/acscatal.3c05656.s001
https://figshare.com/articles/journal_contribution/Broad_Spectrum_Enantioselective_Amide_Bond_Synthetase_from_Streptoalloteichus_hindustanus/24953739

المؤلفون: Donggeon Nam (10036518), Antonio Tinoco (3915989), Zhuofan Shen (12035630), Ronald D. Adukure (12035633), Gopeekrishnan Sreenilayam (2254597), Sagar D. Khare (216014), Rudi Fasan (1307055)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Immunology, Infectious Diseases, Plant Biology, Chemical Sciences not elsewhere classified, obtain chemoenzymatic access, aryl amine substrates, >< sub ><, trifluoromethyl amino esters, acceptor carbene donors, carbene donor, amino alcohols, >, work introduces, valuable synthons, trifluoromethylated amines, trifluoromethyl amines, substrate engineering, opposite enantiomers, metalloprotein scaffold, medicinal chemistry, mediated control, include enzyme, hydrogenobacter thermophilus, first example, enzyme could

Relation: https://figshare.com/articles/journal_contribution/Enantioselective_Synthesis_of_Trifluoromethyl_Amines_via_Biocatalytic_N_H_Bond_Insertion_with_Acceptor-Acceptor_Carbene_Donors/19111295

الاتاحة: https://doi.org/10.1021/jacs.1c10750.s001

المساهمون: Cooperstein, L

المصدر: Anal. Biochem. 50: No. 2, 623-31(Dec 1972).; Other Information: Orig. Receipt Date: 30-JUN-73

وصف الملف: Medium: X

URL الوصول: http://www.osti.gov/scitech/biblio/4610837

المؤلفون: Yu-Qing Xiao, Ping Shang, Xing-Yu Chen, Xiao-Qian Pu, Kai-Wen Jiang, Xuan-Feng Jiang

مصطلحات موضوعية: Biochemistry, Neuroscience, Evolutionary Biology, Immunology, Virology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, photoinduced catalytic efficiency, novel molecular structures, nine amine substrates, multicharge electrostatic interaction, azide – alkynes, 73 ev ), reactive oxygen species, oxidative coupling reaction, g , 8 , excellent photocatalytic performance, 1 , multicomponent confined self, e <, reactive radicals, performance enhancement, confined self, photocatalytic yields, photocatalytic mechanism, cycloaddition reaction, click reaction, >< sub, superoxide radical

Relation: https://figshare.com/articles/journal_contribution/Confined_Self-Assembly_of_Anionic_Cu_sub_8_sub_I_sub_14_sub_sup_6_sup_-Type_Supramolecular_Cluster_and_Performance_Enhancement_of_Photo-Oxidation_and_Photo-Click_Reaction/25222503

الاتاحة: https://doi.org/10.1021/acs.chemmater.3c02971.s001
https://figshare.com/articles/journal_contribution/Confined_Self-Assembly_of_Anionic_Cu_sub_8_sub_I_sub_14_sub_sup_6_sup_-Type_Supramolecular_Cluster_and_Performance_Enhancement_of_Photo-Oxidation_and_Photo-Click_Reaction/25222503

المؤلفون: Zhiqiang Deng (532593), Zhenxiang Zhao (642400), Gang He (239353), Gong Chen (198359)

مصطلحات موضوعية: Biophysics, Biochemistry, Evolutionary Biology, Infectious Diseases, Plant Biology, Virology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, sulfonamide group, reaction conditions, δ alkyl, α substituent, Sulfonamide, oxidation, trigger, sulfonyl-protected, δ-, Mechanistic studies, Photoredox-Mediated Mono, sulfonamide N, Unactivated, Remote, Alkyl, Difluorination, alkylamine, photoredox-mediated, Bond, α-, monofluorination selectivity, amine substrates

Relation: https://figshare.com/articles/journal_contribution/Photoredox-Mediated_Mono-_and_Difluorination_of_Remote_Unactivated_Methylene_C_sp_sup_3_sup_H_Bonds_of_i_N_i_Alkyl_Sulfonamides/14460226

الاتاحة: https://doi.org/10.1021/acs.orglett.1c01020.s001

المساهمون: Dolbeare, Frank [5178 Diane La., Livermore, CA 94550]

وصف الملف: Medium: ED; Size: Pages: ([10] p)

URL الوصول: http://www.osti.gov/scitech/servlets/purl/863690

المساهمون: Dolbeare, Frank [5178 Diane La., Livermore, CA 94550]

وصف الملف: Medium: ED

URL الوصول: http://www.osti.gov/scitech/servlets/purl/863356