المؤلفون: Brandon A. Wright, Alessio Regni, Nattawadee Chaisan, Richmond Sarpong

مصطلحات موضوعية: Biochemistry, Microbiology, Cell Biology, Genetics, Molecular Biology, Pharmacology, Biotechnology, Cancer, Hematology, Chemical Sciences not elsewhere classified, stereospecific thietane reduction, highly effective approach, generating synthetic strategies, generally prioritizes disconnections, designing synthetic routes, dearomative buchner cycloaddition, reduce molecular complexity, navigating excess complexity, generating excess complexity, building excess complexity, daphenylline retrosynthetic analysis, step total synthesis, total synthesis, alkaloid daphenylline, traditional bond, strict adherence, strategic bond, powerful bond, membered ring, heptane core

العلاقة: https://figshare.com/articles/journal_contribution/Navigating_Excess_Complexity_Total_Synthesis_of_Daphenylline/24986290Test

الإتاحة: https://doi.org/10.1021/jacs.3c12953.s001Test
https://figshare.com/articles/journal_contribution/Navigating_Excess_Complexity_Total_Synthesis_of_Daphenylline/24986290Test

المؤلفون: Bocheng Chen, Lucas Pagès, Raphaël Dollet, Cyrille Kouklovsky, Sébastien Prévost, Aurélien de la Torre

مصطلحات موضوعية: Biochemistry, Microbiology, Genetics, Molecular Biology, Biotechnology, Evolutionary Biology, Mental Health, Computational Biology, Chemical Sciences not elsewhere classified, using secondary alcohols, simple starting materials, sequential dual catalysis, building molecular complexity, c – n, c –, vic <, remarkably broad, regioselectivity issues, regioselective fashion, one pot, new approach, lewis acid, first nucleophile, carte <, attractive approach

العلاقة: https://figshare.com/articles/journal_contribution/Regio-_and_Chemoselective_Double_Allylic_Substitution_of_Alkenyl_i_vic_i_-Diols/25417290Test

الإتاحة: https://doi.org/10.1021/acs.orglett.4c00495.s001Test

المؤلفون: Qiaoya Zhang, Yinling Li, Yabo Chen, Jiahua Jiang, Yuan Liu, Jiye Luo, Yang Gao, Yanping Huo, Qian Chen, Xianwei Li

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Molecular Biology, Neuroscience, Biotechnology, Developmental Biology, Mental Health, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, exploiting bifunctional α, enable rapid construction, affording polyfunctional heterocycles, versatile haloalkynes, synthetic efficiency, molecular complexity, featuring step, annulation cascade, alcohol haloalkynes, achieved using

العلاقة: https://figshare.com/articles/journal_contribution/Ru_II_-Catalyzed_Divergent_C_H_Alkynylation_Cascade_with_Bifunctional_Alcohol_Haloalkynes/25365677Test

الإتاحة: https://doi.org/10.1021/acs.orglett.4c00283.s001Test

المؤلفون: Modest von Korff, Thomas Sander

المصدر: CHIMIA, Vol 77, Iss 4 (2023)

مصطلحات موضوعية: Molecular complexity, Natural product synthesis, Reactions, Strychnine, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: https://www.chimia.ch/chimia/article/view/6947Test; https://doaj.org/toc/0009-4293Test; https://doaj.org/toc/2673-2424Test

الوصول الحر: https://doaj.org/article/81f51b8035e24072981772947d988b24Test

المؤلفون: Srinivas Beduru, Andrei G. Kutateladze

المصدر: Molecules, Vol 28, Iss 18, p 6549 (2023)

مصطلحات موضوعية: photoassisted synthetic chemistry, ESIPT, polyheterocycles, sulfonamides, molecular complexity, Organic chemistry, QD241-441

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/1420-3049/28/18/6549Test; https://doaj.org/toc/1420-3049Test

الوصول الحر: https://doaj.org/article/a41c8344222a47b3a23316263199c190Test

المؤلفون: Desvals, Arthur, Hoffmann, Norbert

المساهمون: Institut de Chimie Moléculaire de Reims - UMR 7312 (ICMR), Université de Reims Champagne-Ardenne (URCA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-SFR CAP Santé (Champagne-Ardenne Picardie Santé), Université de Reims Champagne-Ardenne (URCA)-Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS)-SFR Condorcet, Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS), Communauté Urbaine du Grand ReimsUniversité de Reims Champagne-Ardenne

المصدر: ISSN: 0004-9425 ; Australian Journal of Chemistry ; https://cnrs.hal.science/hal-04092928Test ; Australian Journal of Chemistry, 2023, 76 (3), pp.117. ⟨10.1071/CH23029⟩.

مصطلحات موضوعية: aromatic compounds, meta or [2 + 3] photocyloaddition, molecular complexity, natural products, ortho or [2 + 2] photocycloaddition, photocycloaddition, spin multiplicity, terpenes, total synthesis, organic synthesis, photochemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry

العلاقة: hal-04092928; https://cnrs.hal.science/hal-04092928Test; https://cnrs.hal.science/hal-04092928/documentTest; https://cnrs.hal.science/hal-04092928/file/Aust%20J%20Chem%202023.pdfTest

الإتاحة: https://doi.org/10.1071/CH23029Test
https://cnrs.hal.science/hal-04092928Test
https://cnrs.hal.science/hal-04092928/documentTest
https://cnrs.hal.science/hal-04092928/file/Aust%20J%20Chem%202023.pdfTest

المؤلفون: Hao-Cong Li, Ke-Yuan Zhao, Yan Tan, Hao-Sen Wang, Wen-Shan Wang, Xiao-Lan Chen, Bing Yu

مصطلحات موضوعية: Biochemistry, Microbiology, Molecular Biology, Biotechnology, Evolutionary Biology, Infectious Diseases, Chemical Sciences not elsewhere classified, sustainable reaction system, broad substrate scope, achieve molecular complexity, acyl oxime esters, acyl difunctionalization, polar crossover, n <, induced β, excellent regioselectivity, effectively applicable

العلاقة: https://figshare.com/articles/journal_contribution/Visible-Light-Promoted_Intermolecular_Acyl_Difunctionalization_of_Alkenes_via_Oxidative_Radical-Polar_Crossover/24530066Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c03121.s001Test
https://figshare.com/articles/journal_contribution/Visible-Light-Promoted_Intermolecular_Acyl_Difunctionalization_of_Alkenes_via_Oxidative_Radical-Polar_Crossover/24530066Test

المؤلفون: Soumya Jyoti Basak, Jyotirmayee Dash

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Computational Biology, Chemical Sciences not elsewhere classified, step cascade reaction, mediated cascade synthesis, affordable base ko, rutaecarpine alkaloid analogues, rutaecarpine alkaloid, sup ><, successfully applied, substituted indole, salient feature, pentacyclic core, multigram scales, molecular complexity, larger scale, economically viable, dihydroquinazolinone ring, >, >- butoxide

العلاقة: https://figshare.com/articles/journal_contribution/Potassium_i_tert_i_-Butoxide-Mediated_Cascade_Synthesis_of_Rutaecarpine_Alkaloid_Analogues_Access_to_Molecular_Complexity_on_Multigram_Scales/24711296Test

الإتاحة: https://doi.org/10.1021/acs.joc.3c01996.s001Test
https://figshare.com/articles/journal_contribution/Potassium_i_tert_i_-Butoxide-Mediated_Cascade_Synthesis_of_Rutaecarpine_Alkaloid_Analogues_Access_to_Molecular_Complexity_on_Multigram_Scales/24711296Test

المؤلفون: Allie W. Guerra, Joshua G. Pierce

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Physiology, Biotechnology, Evolutionary Biology, Ecology, Immunology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, mechanistic studies indicate, increased molecular complexity, carbon centered radical, achiral substrates obtained, accessing building blocks, access enantioenriched scaffolds, photoredox catalyzed c, α ‑ bromoesters, photoredox methodology

العلاقة: https://figshare.com/articles/journal_contribution/Photoredox_Catalyzed_C_sp_sup_3_sup_C_sp_sup_3_sup_Coupling_of_Bromoesters_and_Triethylamine/24886707Test

الإتاحة: https://doi.org/10.1021/acs.joc.3c02394.s001Test
https://figshare.com/articles/journal_contribution/Photoredox_Catalyzed_C_sp_sup_3_sup_C_sp_sup_3_sup_Coupling_of_Bromoesters_and_Triethylamine/24886707Test

المؤلفون: Bo Jiang, Hao-Tian Wang, Zhi-Chao Chen, Wei Du, Ying-Chun Chen

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Biotechnology, Developmental Biology, Infectious Diseases, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, mild catalytic conditions, mechanistically distinct strategy, higher molecular complexity, good functionality tolerance, broad substrate scope, another chiral moiety, allylic etherification sequence, 0 )- π, component reaction exhibits, asymmetric hydroxymethylative etherification, alcohols via pd, cascade vinylogous addition, reaction process, asymmetric hydroalkoxylation, aliphatic alcohols, valuable frameworks, presented herein, lewis base, high levels, control experiments, concurrently introducing, alkoxyl group

العلاقة: https://figshare.com/articles/journal_contribution/Asymmetric_Hydroxymethylative_Etherification_of_1_3-Dienes_with_Isatins_and_Alcohols_via_Pd_0_-_-Lewis_Base_Catalysis/24913554Test

الإتاحة: https://doi.org/10.1021/acscatal.3c05346.s001Test
https://figshare.com/articles/journal_contribution/Asymmetric_Hydroxymethylative_Etherification_of_1_3-Dienes_with_Isatins_and_Alcohols_via_Pd_0_-_-Lewis_Base_Catalysis/24913554Test