المؤلفون: Yongjie Long, Jiahao Shen, Min Shi, Yin Wei

المصدر: Molecules, Vol 30, Iss 1, p 103 (2024)

مصطلحات موضوعية: mechanistic studies, palladium catalyzed, zwitterionic π-allenyl palladium species, cycloaddition, substrate-controlled reaction, DFT calculation, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1420-3049/30/1/103; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/213e230a52154fd3957c183f59101490

المؤلفون: Kaikai Wang, Wenwen Zhou, Jun Jia, Junwei Ye, Mengxin Yuan, Jie Yang, Yonghua Qi, Rongxiang Chen

المصدر: Molecules, Vol 28, Iss 6761, p 6761 (2023)

مصطلحات موضوعية: substrate-controlled, ninhydrin-derived MBH adducts, 3,4-dihydroisoquinolines, cycloaddition, polycyclic frameworks, Diels-Alder reaction, Organic chemistry, QD241-441

Relation: https://www.mdpi.com/1420-3049/28/19/6761; https://doaj.org/toc/1420-3049; https://doaj.org/article/64dda8a4327548c0b91794f668cf61ab

الاتاحة: https://doi.org/10.3390/molecules28196761
https://doaj.org/article/64dda8a4327548c0b91794f668cf61ab

المؤلفون: Meher Prakash (2816941), Rajni Lodhi (8232954), Sampak Samanta (2317552)

مصطلحات موضوعية: Biochemistry, Cell Biology, Genetics, Biotechnology, Developmental Biology, Plant Biology, Michael-initiated ring-expansion re., DBU, fulvene scaffolds, chemical yields, substrate-controlled annulation method, sulfonyl ketimines, eco-friendly method, cyclopenta, chromene, hydrogenation reaction, 3- alkyl-substituted N, 4- alkyl, 4 C sources, Substrate-Controlled Domino Reaction, thiazepine

Relation: https://figshare.com/articles/journal_contribution/Substrate-Controlled_Domino_Reaction_of_i_N_i_Sulfonyl_Ketimines_with_2_Aroyl-1-chlorocyclopropanecarboxylates_Access_to_Cyclopenta_i_c_i_chromenes_and_Benzo_i_f_i_cyclopenta_i_d_i_1_2_thiazepine_Dioxides/14401741

الاتاحة: https://doi.org/10.1021/acs.joc.1c00459.s001

المؤلفون: Young Eum Hyun (11046022), Hong-Rae Kim (6858920), Lak Shin Jeong (1309611)

مصطلحات موضوعية: Biochemistry, Biotechnology, Sociology, Chemical Sciences not elsewhere classified, cyclopropanation, binding, bicyclo, stereoselectively, Nucleoside, Charette, manner, analogue, Stereoselective Cyclopropanation, sugar conformation, Simmons, stereoselective, template, hydroxyl-directed, reagent-controlled, Cyclopropyl-Fused, Carbocyclic, conformer, peroxisome proliferator-activated r., substrate-controlled, conformationally, Stereoselective Synthesis

Relation: https://figshare.com/articles/journal_contribution/Stereoselective_Synthesis_of_i_S_i_-_and_i_N_i_Cyclopropyl-Fused_Carbocyclic_Nucleosides_Using_Stereoselective_Cyclopropanation/14876977

الاتاحة: https://doi.org/10.1021/acs.joc.1c00705.s001

المؤلفون: Xian-Tao Wu (9915596), En-Kai Xiao (9915593), Feng Ma (464499), Jin Yin (219996), Jie Wang (16762), Peng Chen (6514), Yi-Jun Jiang (1710142)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Biotechnology, Ecology, Mental Health, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, Information Systems not elsewhere classified, carbazole rings, substrate-controlled regiodivergent., Fluoroacylated Carbazoles, air atmosphere, orientation rules, metal catalyst, Friedel, pentafluoropropionylated carbazoles, trifluoroacetylated carbazoles

Relation: https://figshare.com/articles/journal_contribution/Substrate-Controlled_Regiodivergent_Synthesis_of_Fluoroacylated_Carbazoles_via_Friedel_Crafts_Acylation/14417443

الاتاحة: https://doi.org/10.1021/acs.joc.1c00473.s001

المؤلفون: Jiuzhong Huang (4114177), Xiaoning Li (581082), Huiling Wen (6622391), Lu Ouyang (1392907), Nianhua Luo (6988025), Jianhua Liao (1393228), Renshi Luo (1944475)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Ecology, Cancer, Inorganic Chemistry, Computational Biology, Biological Sciences not elsewhere classified, reaction conditions, MeOH, alkene, copper acetate, Hydrogen Source, substrate-controlled stereoselectiv., alkyne, Cu

Relation: https://figshare.com/articles/journal_contribution/Substrate-Controlled_Cu_OAc_sub_2_sub_Catalyzed_Stereoselective_Semi-Reduction_of_Alkynes_with_MeOH_as_the_Hydrogen_Source/14461854

الاتاحة: https://doi.org/10.1021/acsomega.1c01083.s001

المؤلفون: Tereza Edlová (10526520), Hana Dvořáková (1677052), Václav Eigner (1590241), Tomáš Tobrman (1677046)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Biotechnology, Computational Biology, Space Science, Chemical Sciences not elsewhere classified, disubstituted cyclobutenones, carbocation-stabilizing group, Substrate-Controlled Regioselective., Disubstituted, bromination reaction, disubstituted cyclobutenes, disubstituted 3- bromocyclobutenes, allylic position

Relation: https://figshare.com/articles/journal_contribution/Substrate-Controlled_Regioselective_Bromination_of_1_2-Disubstituted_Cyclobutenes_An_Application_in_the_Synthesis_of_2_3-Disubstituted_Cyclobutenones/14374098

الاتاحة: https://doi.org/10.1021/acs.joc.1c00261.s001

المؤلفون: Stephan N. Hess (10088994), Xiaobin Mo (1557070), Conny Wirtz (2988141), Alois Fürstner (1610734)

مصطلحات موضوعية: Biochemistry, Marine Biology, Inorganic Chemistry, Chemical Sciences not elsewhere classified, sector, propargylation, dibromo-BINOL-catalyzed, polyether domain, Limaol, Stille, marine origin, introduction, core region, gold-catalyzed spirocyclization, methylene substituents, two-directional approach, term, nonthermodynamic array, C 40-polyketide, Total Synthesis, substrate-controlled allylation

Relation: https://figshare.com/articles/journal_contribution/Total_Synthesis_of_Limaol/13705125

الاتاحة: https://doi.org/10.1021/jacs.0c12948.s001

المؤلفون: Hisashi Yamamoto, 山本 尚

المصدر: MEDCHEM NEWS. 2020, 30(4):201

المؤلفون: Jeyun Jo, Seok-Ho Kim, Young Han, Jae-Hwan Kwak, Hwayoung Yun

المصدر: Molecules; Volume 22; Issue 7; Pages: 1069

مصطلحات موضوعية: asymmetric cyclization, substrate-controlled manner, total synthesis, natural product

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules22071069

الاتاحة: https://doi.org/10.3390/molecules22071069

المؤلفون: Gastón Álvarez Trentini, Sebastián Miguel Richiano, Gonzalo Diego Veiga, Ernesto Schwarz

المصدر: Marine and Petroleum Geology. 104:1-10

مصطلحات موضوعية: 010504 meteorology & atmospheric sciences, Stratigraphy, HARDGROUNDS, Geociencias multidisciplinaria, 010502 geochemistry & geophysics, Oceanography, 01 natural sciences, Ciencias de la Tierra y relacionadas con el Medio Ambiente, Sedimentary depositional environment, Paleontology, DEPOSITIONAL SETTINGS, 0105 earth and related environmental sciences, Trypanites, NON-DEPOSITION VS EROSION, geography, geography.geographical_feature_category, Bioerosion, Geology, CONTROLLING FACTORS, Sedimentary basin, Gastrochaenolites, Cretaceous, Geophysics, SUBSTRATE-CONTROLLED ICHNOFACIES, Sedimentary basin analysis, Economic Geology, Ichnofacies, CIENCIAS NATURALES Y EXACTAS

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1010e3a31d73cbc06d3c5e295176a6cc
https://doi.org/10.1016/j.marpetgeo.2019.03.020

المؤلفون: Seok-Ho Kim, Jeyun Jo, Jae-Hwan Kwak, Hwayoung Yun, Young Taek Han

المصدر: Molecules, Vol 22, Iss 7, p 1069 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry

مصطلحات موضوعية: natural product, Pharmaceutical Science, Review, 010402 general chemistry, substrate-controlled manner, 01 natural sciences, Catalysis, Analytical Chemistry, lcsh:QD241-441, chemistry.chemical_compound, lcsh:Organic chemistry, asymmetric cyclization, Drug Discovery, Physical and Theoretical Chemistry, total synthesis, Biological Products, Natural product, Molecular Structure, 010405 organic chemistry, Organic Chemistry, Enantioselective synthesis, Substrate (chemistry), Total synthesis, Stereoisomerism, Combinatorial chemistry, 0104 chemical sciences, chemistry, Chemistry (miscellaneous), Cyclization, Molecular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e613affb8002a5874b4a4cc5b221432
http://www.mdpi.com/1420-3049/22/7/1069

المؤلفون: 천국화

المساهمون: 김득준, 제약학과

مصطلحات موضوعية: (+)-laurenyne, asymmetric synthesis, asymmetric synthesis“substrate-controlled” alkylation, ring closing olefin metathesis, “substrate-controlled” alkylation

وصف الملف: 29장.

Relation: http://dcollection.snu.ac.kr:80/jsp/common/DcLoOrgPer.jsp?sItemId=000000043578; https://hdl.handle.net/10371/18032

الاتاحة: https://hdl.handle.net/10371/18032
http://dcollection.snu.ac.kr:80/jsp/common/DcLoOrgPer.jsp?sItemId=000000043578

المؤلفون: Harder, Sjoerd, Spielmann, Jan

المصدر: Harder , S & Spielmann , J 2012 , ' Calcium-mediated hydroboration of alkenes : "Trojan horse" or "true" catalysis? ' , Journal of Organometallic Chemistry , vol. 698 , pp. 7-14 . https://doi.org/10.1016/j.jorganchem.2011.09.025

مصطلحات موضوعية: Calcium, Hydroboration, Borate complexes, Catalysis, SUBSTRATE-CONTROLLED DIASTEREOSELECTIVITIES, ALLYLIC ALCOHOL DERIVATIVES, GROUP METAL-CATALYSTS, STYRENE POLYMERIZATION, PROMOTED HYDROBORATIONS, BENZYLCALCIUM COMPLEXES, RHODIUM COMPLEXES, LIGANDS, CATECHOLBORANE, BOROHYDRIDE

الاتاحة: https://hdl.handle.net/11370/bde7910e-bb61-46fd-9201-8f56b45a8e07
https://research.rug.nl/en/publications/bde7910e-bb61-46fd-9201-8f56b45a8e07
https://doi.org/10.1016/j.jorganchem.2011.09.025

المؤلفون: Jan Spielmann, Sjoerd Harder

المساهمون: Stratingh Institute of Chemistry, Molecular Inorganic Chemistry

المصدر: Journal of Organometallic Chemistry, 698, 7-14. Elsevier Science

مصطلحات موضوعية: BENZYLCALCIUM COMPLEXES, Chemie, Borohydride, Biochemistry, Medicinal chemistry, Catalysis, Inorganic Chemistry, chemistry.chemical_compound, Borate complexes, Hydroboration, Materials Chemistry, Organic chemistry, STYRENE POLYMERIZATION, Physical and Theoretical Chemistry, BOROHYDRIDE, PROMOTED HYDROBORATIONS, Calcium hydride, GROUP METAL-CATALYSTS, Organic Chemistry, ALLYLIC ALCOHOL DERIVATIVES, RHODIUM COMPLEXES, Decomposition, chemistry, CATECHOLBORANE, Calcium, SUBSTRATE-CONTROLLED DIASTEREOSELECTIVITIES, LIGANDS, Nonane, Catecholborane, Stoichiometry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff68a19ed73351a55167b746f4ffcc0c
https://research.rug.nl/en/publications/bde7910e-bb61-46fd-9201-8f56b45a8e07

المؤلفون: Schwarz, Ernesto, Buaotis, L.

المساهمون: Bádenas, Beatriz, Aurell, Marcos, Alonso Zarza, Ana María

مصطلحات موضوعية: Substrate-controlled ichnofacies, Marine sequence boundary, Mulichinco Fm (Valanginian), Neuquén Basin (Argentina), https://purl.org/becyt/ford/1.5, https://purl.org/becyt/ford/1

جغرافية الموضوع: Internacional

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/url/https://www.sedimentologists.org/ims; http://hdl.handle.net/11336/236228; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/236228

المؤلفون: Richiano, Sebastián Miguel, Schwarz, Ernesto, Veiga, Gonzalo Diego, Álvarez Trentini, Gastón

مصطلحات موضوعية: CONTROLLING FACTORS, DEPOSITIONAL SETTINGS, HARDGROUNDS, NON-DEPOSITION VS EROSION, SUBSTRATE-CONTROLLED ICHNOFACIES, https://purl.org/becyt/ford/1.5, https://purl.org/becyt/ford/1

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0264817219301102; http://hdl.handle.net/11336/110172; Richiano, Sebastián Miguel; Schwarz, Ernesto; Veiga, Gonzalo Diego; Álvarez Trentini, Gastón; Non-depositional and erosional “offshore” bioeroded hardgrounds from the Lower Cretaceous of the Neuquén Basin, Argentina: Insights into their sequence-stratigraphic implications and controls; Elsevier; Marine And Petroleum Geology; 104; 6-2019; 1-10; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/110172