المؤلفون: Issa Yavari, Sina Shaabanzadeh, Kiyana Ghafouri

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Genetics, Molecular Biology, Computational Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, scale synthesis along, previous challenging methods, novel electrochemical approach, drug candidate molecules, cyclic voltammetry spectra, scalable diastereoselective electrosynthesis, ones spirobenzofuran scaffolds, protocol compared, mechanistic cognizance, high diastereoselectivity, dimensional structure, convenient accessibility, constant current, achieving spirobenzofurans

Relation: https://figshare.com/articles/journal_contribution/Scalable_Diastereoselective_Electrosynthesis_of_Spiro_benzofuran-2_2_-furan_-3-ones/24794649

الاتاحة: https://doi.org/10.1021/acs.joc.3c02186.s001
https://figshare.com/articles/journal_contribution/Scalable_Diastereoselective_Electrosynthesis_of_Spiro_benzofuran-2_2_-furan_-3-ones/24794649

المؤلفون: Yu-Lin Lu, Yu-Han Qin, Shao-Ping Zheng, Jia Ruan, Yin-Hui Huang, Xiao-Dong Zhang, Chen-Hui Liu, Peng Hu, Hai-Sen Xu, Cheng-Yong Su

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Pharmacology, Biotechnology, Evolutionary Biology, Inorganic Chemistry, Chemical Sciences not elsewhere classified, threefold rate enhancement, sevenfold increase owing, reaction acceleration contributed, mediated allosteric catalysis, known hofmeister effect, kinetic experiments reveal, greatly enhanced yield, efficient allosteric catalysis, >- hh product, mimicking cage catalysis, enzymatic cage effect, high diastereoselectivity anions, amine cage, work highlights, thermodynamic unfavored, syn <, structural allostery, stability due, notable influence, flexible metallo, flexible cages, five cycles

Relation: https://figshare.com/articles/journal_contribution/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787314

الاتاحة: https://doi.org/10.1021/acscatal.3c04593.s001
https://figshare.com/articles/journal_contribution/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787314

المؤلفون: Yiwen Xia, Meng Tang, Qian Zhang, Wentao Yu

مصطلحات موضوعية: Biophysics, Biochemistry, Pharmacology, Biotechnology, Developmental Biology, Cancer, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, stereoselective synthesis, stereoselective preparation, high diastereoselectivity, efficient formation, 3 ‑<, 3 -<

Relation: https://figshare.com/articles/journal_contribution/Dearomatization_of_Pyridines_Stereoselective_Synthesis_of_Functionalized_1_2_4_Triazolo_4_3_i_a_i_pyridines/24866847

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03060.s001
https://figshare.com/articles/journal_contribution/Dearomatization_of_Pyridines_Stereoselective_Synthesis_of_Functionalized_1_2_4_Triazolo_4_3_i_a_i_pyridines/24866847

المؤلفون: Hiyori Takebe (14321591), Nana Yoshino (8879105), Yukako Shimada (218388), Craig M. Williams (1939036), Seijiro Matsubara (1490731)

مصطلحات موضوعية: Medicine, Molecular Biology, Neuroscience, Pharmacology, Evolutionary Biology, Ecology, Inorganic Chemistry, Mental Health, Infectious Diseases, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, first diastereoselective synthesis, establish chirality within, electrophilic trapping afforded, cubane carboxylic acid, chiral amide followed, >- selective deprotonations, selective deprotonation, cubane skeleton, chiral auxiliary, trisubstituted cubanes, ready conversion, ortho <, high diastereoselectivity, enriched cubanes, directed site, corresponding 1, appropriate positions, achieved using

Relation: https://figshare.com/articles/journal_contribution/Chiral_Auxiliary-Directed_Site-Selective_Deprotonation_of_the_Cubane_Skeleton/21806708

الاتاحة: https://doi.org/10.1021/acs.orglett.2c03659.s001

المؤلفون: Dmitry Dar’in (1555282), Grigory Kantin (6448364), Daria Glushakova (14334845), Vladimir Sharoyko (8535474), Mikhail Krasavin (820851)

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Pharmacology, Ecology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, – h insertion, thereby demonstrating quite, ii )- catalyzed, diazocarbonyl compounds suitable, propiolic acids though, propiolic acids followed, generally high yields, promoted cyclization 3, like spirocyclic δ, diazotetramic acids, like δ, high diastereoselectivity, virtually insensitive, valid substrates, target δ, somewhat sensitive, new class, monosubstituted 3, large scope, chiral 5, approach outlined

Relation: https://figshare.com/articles/journal_contribution/Diazo_Tetramic_Acids_Provide_Access_to_Natural-Like_Spirocyclic_sup_sup_-Butenolides_through_Rh_II_-Catalyzed_O_H_Insertion_Base-Promoted_Cyclization/21824771

الاتاحة: https://doi.org/10.1021/acs.joc.2c02600.s001

المؤلفون: Ali Nikbakht (4545577), Ahmadreza Ebrahimi Valdani (14289843), Hossein Zahedian Tejeneki (10646109), Alireza Abbasi Kejani (10097803), Nahid S. Alavijeh (14289846), Felix Bauer (2025250), Fatemeh Darvish (1938883), Bernhard Breit (1444627), Saeed Balalaie (1754095)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Microbiology, Cell Biology, Genetics, Molecular Biology, Physiology, Ecology, Developmental Biology, Infectious Diseases, Plant Biology, Computational Biology, diastereoselective cascade annulation, 38 – 93, possible reaction pathway, reaction proceeds, unprecedented non, unexpected rearrangement, situ <, rearomatized rearrangement, n <, high diastereoselectivity, generated isoquinoline, broad range, bridged heterocycles, allows access

Relation: https://figshare.com/articles/journal_contribution/A_Diastereoselective_Cascade_Annulation_Approach_to_Bridged_Polycyclic_Heterocycles_Involving_an_Unexpected_Rearrangement/21764142

الاتاحة: https://doi.org/10.1021/acs.orglett.2c03629.s001

المؤلفون: Shengquan Duan (1857154), Daniel W. Widlicka (1413220), Michael P. Burns (11382574), Rajesh Kumar (72124), Ian Hotham (11382577), Jean-Nicolas Desrosiers (1392826), Paul Bowles (1458148), Kris N. Jones (1857169), Lindsay D. Nicholson (11382580), Michele T. Buetti-Weekly (11382583), Lu Han (151620), Jeremy Steflik (1292913), Eric Hansen (2337007), Cheryl M. Hayward (1997578), Holly Strohmeyer (1857070), Sébastien Monfette (11382586), Scott C. Sutton (2025337), Christopher Morris (92583)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Marine Biology, Infectious Diseases, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, substituted chiral amines, enzymatic reductive amination, engineered imine reductase, chiral secondary amine, catalyzed reductive cyclization, biocatalytic reductive amination, n , 3 , process development, powerful tool, key intermediate, high diastereoselectivity, cdk 2, also presented, 6 inhibitor

Relation: https://figshare.com/articles/journal_contribution/Application_of_Biocatalytic_Reductive_Amination_for_the_Synthesis_of_a_Key_Intermediate_to_a_CDK_2_4_6_Inhibitor/16566430

الاتاحة: https://doi.org/10.1021/acs.oprd.1c00255.s001

المؤلفون: Dongqiu Li (11740272), Fang Cheng (138729), Yuhai Tang (1819468), Jing Li (10611), Yang Li (7082), Jiao Jiao (297582), Silong Xu (1819465)

مصطلحات موضوعية: Biochemistry, Medicine, Molecular Biology, Biotechnology, Sociology, Environmental Sciences not elsewhere classified, highly functionalized cyclohexenes, catalyzed internal redox, c ­( sp, deficient alkenes herein, deficient alkenes, reaction offers, mild conditions, high diastereoselectivity, good yields, formally oxidized, exclusive regioselectivity, efficient synthesis, alkynyl moiety

Relation: https://figshare.com/articles/journal_contribution/Phosphine-Catalyzed_Internal_Redox_4_2_Annulation_between_1_4-Enynoates_and_Electron-Deficient_Alkenes/17062386

الاتاحة: https://doi.org/10.1021/acs.orglett.1c03206.s001

المؤلفون: Russell Shelp (11840441), Rohan R. Merchant (1378866), Jonathan M. E. Hughes (6912470), Patrick J. Walsh (304213)

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Molecular Biology, Sociology, Infectious Diseases, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, key levocetirizine intermediate, controlled silane addition, 1 ]­ pentane, 2 , 1 ]­ propellane, sulfinimine addition, streamlined synthesis, strategic impact, stereoselective synthesis, reaction initiation, mh hat, mechanistic evidence, high diastereoselectivity, evolution pathway, demonstrated via, competitive h, benzylamine derivatives

Relation: https://figshare.com/articles/journal_contribution/Enantioenriched_BCP_Benzylamine_Synthesis_via_Metal_Hydride_Hydrogen_Atom_Transfer_Sulfinimine_Addition_to_1_1_1_Propellane/17207237

الاتاحة: https://doi.org/10.1021/acs.orglett.1c03681.s001

المؤلفون: Yu-Lin Lu, Yu-Han Qin, Shao-Ping Zheng, Jia Ruan, Yin-Hui Huang, Xiao-Dong Zhang, Chen-Hui Liu, Peng Hu, Hai-Sen Xu, Cheng-Yong Su

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Pharmacology, Biotechnology, Evolutionary Biology, Inorganic Chemistry, Chemical Sciences not elsewhere classified, threefold rate enhancement, sevenfold increase owing, reaction acceleration contributed, mediated allosteric catalysis, known hofmeister effect, kinetic experiments reveal, greatly enhanced yield, efficient allosteric catalysis, >- hh product, mimicking cage catalysis, enzymatic cage effect, high diastereoselectivity anions, amine cage, work highlights, thermodynamic unfavored, syn <, structural allostery, stability due, notable influence, flexible metallo, flexible cages, five cycles

Relation: https://figshare.com/articles/dataset/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787323

الاتاحة: https://doi.org/10.1021/acscatal.3c04593.s004
https://figshare.com/articles/dataset/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787323

المؤلفون: Yu-Lin Lu, Yu-Han Qin, Shao-Ping Zheng, Jia Ruan, Yin-Hui Huang, Xiao-Dong Zhang, Chen-Hui Liu, Peng Hu, Hai-Sen Xu, Cheng-Yong Su

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Pharmacology, Biotechnology, Evolutionary Biology, Inorganic Chemistry, Chemical Sciences not elsewhere classified, threefold rate enhancement, sevenfold increase owing, reaction acceleration contributed, mediated allosteric catalysis, known hofmeister effect, kinetic experiments reveal, greatly enhanced yield, efficient allosteric catalysis, >- hh product, mimicking cage catalysis, enzymatic cage effect, high diastereoselectivity anions, amine cage, work highlights, thermodynamic unfavored, syn <, structural allostery, stability due, notable influence, flexible metallo, flexible cages, five cycles

Relation: https://figshare.com/articles/dataset/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787317

الاتاحة: https://doi.org/10.1021/acscatal.3c04593.s002
https://figshare.com/articles/dataset/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787317

المؤلفون: Yu-Lin Lu, Yu-Han Qin, Shao-Ping Zheng, Jia Ruan, Yin-Hui Huang, Xiao-Dong Zhang, Chen-Hui Liu, Peng Hu, Hai-Sen Xu, Cheng-Yong Su

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Pharmacology, Biotechnology, Evolutionary Biology, Inorganic Chemistry, Chemical Sciences not elsewhere classified, threefold rate enhancement, sevenfold increase owing, reaction acceleration contributed, mediated allosteric catalysis, known hofmeister effect, kinetic experiments reveal, greatly enhanced yield, efficient allosteric catalysis, >- hh product, mimicking cage catalysis, enzymatic cage effect, high diastereoselectivity anions, amine cage, work highlights, thermodynamic unfavored, syn <, structural allostery, stability due, notable influence, flexible metallo, flexible cages, five cycles

Relation: https://figshare.com/articles/dataset/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787320

الاتاحة: https://doi.org/10.1021/acscatal.3c04593.s003
https://figshare.com/articles/dataset/Anion-Mediated_Allosteric_Catalysis_of_2_2_Photocycloaddition_Based_on_a_Flexible_Metallo-Amine_Cage_for_High_Diastereoselectivity/24787320

المؤلفون: Yiwen Xia, Meng Tang, Qian Zhang, Wentao Yu

مصطلحات موضوعية: Biophysics, Biochemistry, Pharmacology, Biotechnology, Developmental Biology, Cancer, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, stereoselective synthesis, stereoselective preparation, high diastereoselectivity, efficient formation, 3 ‑<, 3 -<

Relation: https://figshare.com/articles/dataset/Dearomatization_of_Pyridines_Stereoselective_Synthesis_of_Functionalized_1_2_4_Triazolo_4_3_i_a_i_pyridines/24866850

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03060.s002
https://figshare.com/articles/dataset/Dearomatization_of_Pyridines_Stereoselective_Synthesis_of_Functionalized_1_2_4_Triazolo_4_3_i_a_i_pyridines/24866850

المؤلفون: Babayan, E. P.

المصدر: Proceedings of the YSU B: Chemical and Biological Sciences; Vol. 40 No. 2 (210) (2006); 91-96 ; ԵՊՀ Գիտական տեղեկագիր. Քիմիական և կենսաբանական գիտություններ; Vol. 40 No. 2 (210) (2006); 91-96 ; ԵՊՀ Գիտական տեղեկագիր. Քիմիա և կենսաբանություն; Vol. 40 No. 2 (210) (2006); 91-96 ; Ученые записки ЕГУ: химические и биологические науки; Том 40 № 2 (210) (2006); 91-96 ; 2953-7983 ; 1829-1767 ; 10.46991/PYSU:B\2006.40.2

مصطلحات موضوعية: Schiffs base, Ni(II) complex, $\alpha$-bromacrylic acid, high diastereoselectivity, X-ray structural method

وصف الملف: application/pdf

Relation: https://journals.ysu.am/index.php/proceedings-chem-biol/article/view/vol40_no2_2006_pp091-096/pdf; https://journals.ysu.am/index.php/proceedings-chem-biol/article/view/vol40_no2_2006_pp091-096

الاتاحة: https://journals.ysu.am/index.php/proceedings-chem-biol/article/view/vol40_no2_2006_pp091-096
https://doi.org/10.46991/PYSU:B/2006.40.2.091

المؤلفون: Dmitry Dar’in, Grigory Kantin, Daria Glushakova, Vladimir Sharoyko, Mikhail Krasavin

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Pharmacology, Ecology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, – h insertion, thereby demonstrating quite, ii )- catalyzed, diazocarbonyl compounds suitable, propiolic acids though, propiolic acids followed, generally high yields, promoted cyclization 3, like spirocyclic δ, diazotetramic acids, like δ, high diastereoselectivity, virtually insensitive, valid substrates, target δ, somewhat sensitive, new class, monosubstituted 3, large scope, chiral 5, approach outlined

Relation: https://doi.org/10.1021/acs.joc.2c02600.s001

الاتاحة: https://doi.org/10.1021/acs.joc.2c02600.s001

المؤلفون: Martínez Bonilla, Carlos A., Puerto Galvis, Carlos E., Vargas Mendez, Leonor Y., Kouznetsov, Vladimir V.

مصطلحات موضوعية: High diastereoselectivity, Synthesis of Tetrahydroquinolines, Toxicity, Embryos

جغرافية الموضوع: CRAI-USTA Bogotá

وصف الملف: application/pdf

Relation: For a detailed review in the field see: V. Sridharan, P. A. Suryavanshi, J. C. Menéndez, Chem. Rev., 2011, 111, 7157.; (a) A. Hagfeldt, G. Boschloo, L. Sun, L. Kloo, H. Pettersson, Chem. Rev., 2010, 110, 6595; (b) R. Chen, X. Yang, H. Tian, X. Wang, A. Hagfeldt, L. Sun, Chem. Mater., 2007, 19, 4007; (c) Y. Hao, X. Yang, J. Cong, A. Hagfeldt, L. Sun, Tetrahedron, 2012, 68, 552; (d) K. Rakstys, J. Solovjova, T. Malinauskas, I. Bruder, R. Send, A. Sackus, R. Sens, V. Getautis, Dye Pigment., 2014, 104, 211.; R. J. Pagliero, S. Lusvarghi, A. B. Pierini, R. Brun, M. R. Mazzieri, Bioorg. Med. Chem., 2010, 18, 142.; R. N. Asolkar, D. Schröder, R. Heckmann, S. Lang, I. Wagner- Döbler, H. Laatsch, J. Antibiot., 2004, 57, 17.; R. Hiessböck, C. Wolf, E. Richter, M. Hitzler, P. Chiba, M. Kratzel, G. Ecker, J. Med. Chem., 1999, 42, 1921.; J. Liu, Y. Wang, Y. Sun, D. Marshall, S. Miao, G. Tonn, P. Anders, J. Tocker, H. L. Tang, J. Medina, Bioorg. Med. Chem. Lett., 2009, 19, 6840.; W. A. Kinney, C. A. Teleha, A. S. Thompson, M. Newport, R. Hansen, S. Ballentine, S. Ghosh, A. Mahan, G. Grasa, A. Zanotti-Gerosa, J. Dingenen, C. Schubert, Y. Zhou, G. C. Leo, D. F. McComsey, R. J. Santulli, B. E. Maryanoff, J. Org. Chem., 2008, 73, 2302.; G. Li, J. Ren, P. Yao, Y. Duan, H. Zhang, Q. Wu, J. Feng, P. C. K. Lau, D. Zhu, ACS Catal., 2014, 4, 903.; (a) H-G. Imrich, J. Conrad, D. Bubrin, U. Beifuss, J. Org. Chem., 2015, 80, 2319. (b) C. R. Borel, L. C. Almeida Barbosa, C. R. Álvares Maltha, S. A. Fernandes, Tetrahedron Lett., 2015, 56, 662.; (a) D. R. Merchán Arenas, V. V. Kouznetsov, J. Org. Chem., 2014, 79, 5327; (b) V. V. Kouznetsov, Tetrahedron, 2009, 65, 2721; (c) S. Kobayashi, H. Ishitani, S. Nagayama, Synthesis, 1995, 1195.; G. Masson, C. Lalli, M. Benohouda, G. Dagousseta, Chem. Soc. Rev., 2013, 42, 902.; D. Tejedor, F. García-Tellado, Chem. Soc. Rev., 2007, 36, 484.; V. V. Kouznetsov, D. R. Merchán Arenas, C. Ortiz Areniz, C. Meléndez Gómez, Synthesis, 2011, 4011.; D. R. Merchán Arenas, C. A. Martínez Bonilla, V. V Kouznetsov, Org. Biomol. Chem., 2013, 11, 3655.; S. Basu, C. Sachidanandan, Chem. Rev., 2013, 113, 7952.; V. E. Fako, D. Y. Furgeson, Adv. Drug Delivery Rev., 2009, 61, 478.; (a) C. E. Puerto Galvis, V. V. Kouznetsov, Org. Biomol. Chem., 2013, 11, 407; (b) C. E. Puerto Galvis, V. V. Kouznetsov, Org. Biomol. Chem., 2013, 11, 7372.; V. Sridharan, C. Avendaño, J. C. Menéndez, Tetrahedron, 2007, 63, 673.; V. Sridharan, J. C. Menéndez, Chem. Rev., 2010, 110, 3805.; K. Karnakar, J. Shangkar, S. N. Murthy, K. Ramesch, Y. V. D. Nageshwar, Synlett, 2011, 1089.; http://hdl.handle.net/11634/20117; https://doi.org/10.1039/C6RA04325A

الاتاحة: http://hdl.handle.net/11634/20117
https://doi.org/10.1039/C6RA04325A

المؤلفون: Loh, T.-P., Huang, J.-M., Xu, K.-C., Goh, S.-H., Vittal, J.J.

المساهمون: CHEMISTRY

المصدر: Scopus

مصطلحات موضوعية: 1,3-amino alcohols, Allylation, High diastereoselectivity, Indium, Remote substituent

Relation: Loh, T.-P.,Huang, J.-M.,Xu, K.-C.,Goh, S.-H.,Vittal, J.J. (2000-08-12). A remote substituent as a control element in indium-mediated allylation reactions in aqueous media: Highly diastereoselective synthesis of 1,3-amino alcohols. Tetrahedron Letters 41 (33) : 6511-6515. ScholarBank@NUS Repository.; http://scholarbank.nus.edu.sg/handle/10635/75480; NOT_IN_WOS

الاتاحة: http://scholarbank.nus.edu.sg/handle/10635/75480

المؤلفون: Hongming Cui, Daizong Lin, Dang Qun, Xu Bai

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Immunology, Developmental Biology, Virology, Chemical Sciences not elsewhere classified, kinetically controlled conditions, good chemical yields, desired chiral configuration, cyclic phosphonate esters, challenging enantioselective synthesis, dioxaphosphorinane derivatives via, catalyzed coupling reactions, 2 ‑ oxo, dioxaphosphorinane derivatives, coupling reactions, stereoselective synthesis, asymmetric synthesis, widely applied, two epimers, thorough investigation, photoelectric materials, organic chemistry, high diastereoselectivity, h <, experimentally led

Relation: https://figshare.com/articles/journal_contribution/Kinetically_Controlled_Stereoselective_Synthesis_of_2_Oxo-2-aryl-1_3_2-dioxaphosphorinane_Derivatives_via_a_Palladium-Catalyzed_Reaction/25224130

الاتاحة: https://doi.org/10.1021/acs.joc.3c02151.s001
https://figshare.com/articles/journal_contribution/Kinetically_Controlled_Stereoselective_Synthesis_of_2_Oxo-2-aryl-1_3_2-dioxaphosphorinane_Derivatives_via_a_Palladium-Catalyzed_Reaction/25224130

المؤلفون: Paras J. Patel (14278979), Divyang M. Patel (7830626), Ruturajsinh M. Vala (7830629), Subham G. Patel (14278982), Dipti B. Upadhyay (14278985), Yuvaraj Pannerselvam (14278988), Hitendra M. Patel (7830635)

مصطلحات موضوعية: Biochemistry, Biotechnology, Virology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, radical scavenging assays, exhibit excellent potency, environmentally benign approach, easy workup procedure, >- factor values, vitro antioxidant activity, bis ­( 3, synthesized spiro compounds, >]­ quinoline ], 2 ′- azino, 4l , >]­ quinoline, antioxidant study, 3 -<, trans <, g <, f <, e <, cis <, meldrum ’, high diastereoselectivity, final motif, established using, based synthesis, aryl aldehyde

Relation: https://figshare.com/articles/journal_contribution/Catalyst-Free_Room-Temperature_Accessible_Regioselective_Synthesis_of_Spiroquinolines_and_Their_Antioxidant_Study/21751610

الاتاحة: https://doi.org/10.1021/acsomega.2c05020.s001

المؤلفون: Hongming Cui, Daizong Lin, Dang Qun, Xu Bai

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Immunology, Developmental Biology, Virology, Chemical Sciences not elsewhere classified, kinetically controlled conditions, good chemical yields, desired chiral configuration, cyclic phosphonate esters, challenging enantioselective synthesis, dioxaphosphorinane derivatives via, catalyzed coupling reactions, 2 ‑ oxo, dioxaphosphorinane derivatives, coupling reactions, stereoselective synthesis, asymmetric synthesis, widely applied, two epimers, thorough investigation, photoelectric materials, organic chemistry, high diastereoselectivity, h <, experimentally led

Relation: https://figshare.com/articles/journal_contribution/Kinetically_Controlled_Stereoselective_Synthesis_of_2_Oxo-2-aryl-1_3_2-dioxaphosphorinane_Derivatives_via_a_Palladium-Catalyzed_Reaction/25224130

الاتاحة: https://doi.org/10.1021/acs.joc.3c02151.s001