المؤلفون: Hengzhao Li, Yuxia Hou, Mengqi Peng, Lijun Wang, Junyu Li, Lei Ning, Zemin Lai, Yixuan Li, Jie An

المصدر: Molecules; Volume 28; Issue 1; Pages: 416

مصطلحات موضوعية: acyl chlorides, reductive deuteration, α, α -dideuterio alcohols, SmI 2, D 2 O

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules28010416

الاتاحة: https://doi.org/10.3390/molecules28010416

المؤلفون: Suranjan De (4570315), Shmaryahu Hoz (1328931)

مصطلحات موضوعية: Biophysics, Biochemistry, Pharmacology, Biotechnology, Sociology, Mathematical Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, SmI 2, equilibrium constants, amines, additive, ligand, SmI 2 reactions, role, method, Interaction, complexation, Quantitation, Con, Pro, VIS spectroscopy, Amine, correlation, NMR Spectroscopies, samarium iodide

Relation: https://figshare.com/articles/journal_contribution/Quantitation_of_the_Interactions_of_Alcohols_and_Amines_with_SmI_sub_2_sub_Pros_and_Cons_of_VIS_and_NMR_Spectroscopies/15066662

الاتاحة: https://doi.org/10.1021/acs.joc.1c01183.s001

المؤلفون: Soumitra Agasti (2096182), Nicholas A. Beattie (2854259), Joseph J. W. McDouall (8666214), David J. Procter (1298652)

مصطلحات موضوعية: Biophysics, Biochemistry, Sociology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, SmI 2, aryl cyclopropyl ketones, superstoichiometric amounts, electron transfer reductant, reagent SmI 2

Relation: https://figshare.com/articles/journal_contribution/SmI_sub_2_sub_Catalyzed_Intermolecular_Coupling_of_Cyclopropyl_Ketones_and_Alkynes_A_Link_between_Ketone_Conformation_and_Reactivity/14115415

الاتاحة: https://doi.org/10.1021/jacs.1c01356.s001

المؤلفون: Shihui Luo (5179934), Chaoqun Weng (7553843), Zixuan Qin (11216637), Ke Li (106849), Tianxiao Zhao (8306922), Yuxuan Ding (3625970), Chen Ling (389353), Yuan Ma (189824), Jie An (543888)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Developmental Biology, Cancer, Hematology, Computational Biology, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, Deuterated, reductive deuteration strategy, reductive deuteration, CH, CN, nitrile, tandem SmI 2, synthesis

Relation: https://figshare.com/articles/journal_contribution/Tandem_H_D_Exchange-SET_Reductive_Deuteration_Strategy_for_the_Synthesis_of_-Deuterated_Amines_Using_D_sub_2_sub_O/15710721

الاتاحة: https://doi.org/10.1021/acs.joc.1c01276.s001

المؤلفون: Nels T. Anderson (11126151), Joseph C. Wright (11126154), Gregory S. Girolami (1595761)

مصطلحات موضوعية: Biophysics, Biochemistry, Evolutionary Biology, Infectious Diseases, Plant Biology, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, DMADB, DME, Tm II N, SmI 2, BH, Sm II, crystal structures, 11 B NMR data, Thulium N, KC 8, TmI 2, BNMe, III, Tm II complexes, THF results, reaction mixture results, 18- crown -6, Divalent Samarium, IR data, 1 H

Relation: https://figshare.com/articles/journal_contribution/Synthesis_and_Characterization_of_Divalent_Samarium_and_Thulium_i_N_i_i_N_i_Dimethylaminodiboranates/14974581

الاتاحة: https://doi.org/10.1021/acs.inorgchem.1c01139.s001

المؤلفون: Zhumin Zhang (3496247), Zhuojia Xu (10343378), Xingbang Liu (9526135), Shiwei Luo (3308541), Tiehai Li (1574767)

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Molecular Biology, Neuroscience, Biotechnology, Plant Biology, Chemical Sciences not elsewhere classified, β- Kdo C, SmI 2, Stereoselective Synthesis, anomeric aminopropyl linker, peracetylated anomeric acetate, Reformatsky reactions, anomeric 2- pyridyl sulfide, carbonyl compounds, oct -2-ulosonic

Relation: https://figshare.com/articles/journal_contribution/Stereoselective_Synthesis_of_i_C_i_Glycosides_of_3_Deoxy_d-_i_manno_i_-oct-2-ulosonic_Acid_Kdo_via_SmI_sub_2_sub_Mediated_Reformatsky_Reactions/15044084

الاتاحة: https://doi.org/10.1021/acs.orglett.1c02158.s001

المؤلفون: Lei Ning (7550786), Hengzhao Li (3625958), Zemin Lai (8267760), Michal Szostak (1305681), Xingyue Chen (9623386), Yanhong Dong (160938), Shuhui Jin (4278619), Jie An (543888)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Developmental Biology, Space Science, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, SmI 2, D 2 O, tebufenpyrad analogue, Deuterium Source, Reductive Deuteration, amines, synthesis, protocol exhibits, building blocks, single-electron-transfer reductive ., deuterium atom, α- position, electron donor

Relation: https://figshare.com/articles/journal_contribution/Synthesis_of_Deuterated_Primary_Amines_i_via_i_Reductive_Deuteration_of_Oximes_Using_D_sub_2_sub_O_as_a_Deuterium_Source/13637117

الاتاحة: https://doi.org/10.1021/acs.joc.0c02829.s001

المؤلفون: Shicheng Shi, Michal Szostak

المصدر: Molecules; Volume 22; Issue 11; Pages: 2018

مصطلحات موضوعية: samarium iodide, nitrogen heterocycles, nitrogen, radicals, reductive coupling, SmI 2, radical cyclizations, samarium diiodide, umpolung cyclizations, aminoketyl radicals

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules22112018

الاتاحة: https://doi.org/10.3390/molecules22112018

المؤلفون: Soumitra Agasti, Nicholas A. Beattie, Joseph J. W. McDouall, David J. Procter

مصطلحات موضوعية: Biophysics, Biochemistry, Sociology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, SmI 2, aryl cyclopropyl ketones, superstoichiometric amounts, electron transfer reductant, reagent SmI 2, info, socio

Relation: https://doi.org/10.1021/jacs.1c01356.s001

الاتاحة: https://doi.org/10.1021/jacs.1c01356.s001

المؤلفون: Department of Chemistry, University of Florida Gainesville, FL 32611, USA ( host institution ), Enholm, Eric J. ( author ), Trivellas, Antigone ( author )

مصطلحات موضوعية: SmI 2, tandem cyclizations, carbohydrates, carbocycles

وصف الملف: Pages 1627-1628

Relation: Tetrahedron Letters; 0040-4039(94)88303-3; TETL; http://ufdc.ufl.edu/LS00510273/00001

الاتاحة: https://doi.org/10.1016/0040-4039(94)88303-3
http://ufdc.ufl.edu/LS00510273/00001

المؤلفون: Department of Chemistry, University of Florida Gainesville, Florida 32611, U.S.A. ( host institution ), Enholm, Eric J. ( author ), Jiang, Shujun ( author )

مصطلحات موضوعية: ketyl, SmI 2, carbohydrate lactone, (+)-dihydrocarvone, (−)-menthone

وصف الملف: Pages 6069-6072

Relation: Tetrahedron Letters; S0040-4039(00)60008-4; TETL; http://ufdc.ufl.edu/LS00510269/00001

الاتاحة: https://doi.org/10.1016/S0040-4039(00)60008-4
http://ufdc.ufl.edu/LS00510269/00001

المؤلفون: Xianhuang Zeng (3335322), Dale L. Boger (1306542)

مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Molecular Biology, Physiology, Marine Biology, Cancer, Plant Biology, Chemical Sciences not elsewhere classified, BF, cyclization, SmI 2, acyl α- aminoalkyl, indole, quaternary center, core structure, bond, synthesis, Strempeliopine, dearomative transannular, OEt, formation, Total Synthesis, iminium ion, electron reduction

Relation: https://figshare.com/articles/journal_contribution/Total_Synthesis_of_-Strempeliopine/15078930

الاتاحة: https://doi.org/10.1021/jacs.1c06913.s001

المؤلفون: Moritz J. Classen (10886182), Markus N. A. Böcker (10886185), Remo Roth (6243278), Willi M. Amberg (10886188), Erick M. Carreira (1330920)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Physiology, Marine Biology, Plant Biology, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, Enantioselective, generation, ingenane-derived, SmI 2, diastereoselectivity, Access, euphorikanin, tetracyclic skeleton, vinyl lithium species, implementation, ring B, intramolecular attack, approach, Synthesi, polarity-reversed cyclization proceeds, α- ketolactone, chemoselective transformations, ketyl, synthesis

Relation: https://figshare.com/articles/journal_contribution/Enantioselective_Total_Synthesis_of_-Euphorikanin_A/14691289

الاتاحة: https://doi.org/10.1021/jacs.1c04210.s001