المؤلفون: Jones, Kerry E, Lara, Fernando Martínez, Zavesky, Blane P, Sarpong, Richmond

مصطلحات موضوعية: Organic Chemistry, Chemical Sciences, Total synthesis, Scholarinine A, Oxidative coupling, Alkaloids' akuammiline, Indole, Alkaloids’ akuammiline, Medicinal and Biomolecular Chemistry, Biochemistry and cell biology, Medicinal and biomolecular chemistry, Organic chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9m60098f
https://escholarship.org/content/qt9m60098f/qt9m60098f.pdf

المؤلفون: Naoki Hashimoto, Junichi Taguchi, Norihito Arichi, Shinsuke Inuki, Hiroaki Ohno

مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Biotechnology, Infectious Diseases, Chemical Sciences not elsewhere classified, quaternary carbon center, catalyzed cyclization reaction, bulky tips group, cyclization controlled, carboxy group, tricyclic indoline, stereoselective construction, resulting imine, reductively cleaved, nucleophilic attack, lactone moiety, fused indolines, fused indoline, dig <, akuammiline alkaloids

Relation: https://figshare.com/articles/journal_contribution/Gold_I_-Catalyzed_Cascade_Cyclization_of_Alkynyl_Indoles_for_the_Stereoselective_Construction_of_the_Quaternary_Carbon_Center_of_Akuammiline_Alkaloids/24749094

الاتاحة: https://doi.org/10.1021/acs.joc.3c02142.s001
https://figshare.com/articles/journal_contribution/Gold_I_-Catalyzed_Cascade_Cyclization_of_Alkynyl_Indoles_for_the_Stereoselective_Construction_of_the_Quaternary_Carbon_Center_of_Akuammiline_Alkaloids/24749094

المؤلفون: Chun-Hoe Tan (7533455), Joanne Soon-Yee Yeap (4556467), Siew-Huah Lim (1426534), Yun-Yee Low (1426531), Kae-Shin Sim (666138), Toh-Seok Kam (1426537)

مصطلحات موضوعية: Biochemistry, Cell Biology, Genetics, Pharmacology, Biotechnology, Developmental Biology, Cancer, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Tubulin Polymerization, compound, mitochondrial apoptosis, antiproliferative activity, macroline-akuammiline bisindole, HT -29 Cells, Compounds 1, Alstonia penangiana, Taxol-binding site, spectroscopic data, angustilongine M, macroline-sarpagine bisindole, tubulin polymerization assays, Alstonia penangiana Induce Mitochon., time-dependent manner, Bisindole Alkaloids Angustilongines M, docking analysis, cancer cell lines, β- tubulin subunit, HT -29 spheroids, microtubule-stabilizing agents

Relation: https://figshare.com/articles/journal_contribution/The_Bisindole_Alkaloids_Angustilongines_M_and_A_from_i_Alstonia_penangiana_i_Induce_Mitochondrial_Apoptosis_and_G0_G1_Cell_Cycle_Arrest_in_HT-29_Cells_through_Promotion_of_Tubulin_Polymerization/14448133

الاتاحة: https://doi.org/10.1021/acs.jnatprod.1c00013.s001

المؤلفون: Hoang, Anita

مصطلحات موضوعية: total synthesis, indole alkaloids, Domino reactions, vicinal quaternary stereocenters, quaternary stereocenter, indoline synthesis, communesin alkaloid, perophoramidine, dehaloperophoramidine, akuammiline alkaloids, strictamine, intramolecular Heck reaction, domino carbopalladation carbonylation, indoline alkaloids, Naturvetenskap, Natural Sciences, Kemi, Organisk kemi, Chemical Sciences, Organic Chemistry

وصف الملف: electronic

URL الوصول: https://lup.lub.lu.se/record/a5028c19-1f57-454c-92e3-fecd8a5b8bf3
https://portal.research.lu.se/files/61838631/Doctoral_thesis_final_2_.pdf

المؤلفون: Adizov, Shahobiddin, Tashkhodjaev, Bakhodir

المصدر: European Journal of Chemistry; Vol. 10 No. 4 (2019): December 2019; 345-349 ; 2153-2257 ; 2153-2249

مصطلحات موضوعية: Chirality, Akuammine, Akuammiline, Indole alkaloids, Absolute configuration, Single crystal structure

وصف الملف: application/pdf; text/plain

Relation: https://www.eurjchem.com/index.php/eurjchem/article/view/1898/pdf_1898; https://www.eurjchem.com/index.php/eurjchem/article/view/1898/2626; https://www.eurjchem.com/index.php/eurjchem/article/view/1898

الاتاحة: https://www.eurjchem.com/index.php/eurjchem/article/view/1898
https://doi.org/10.5155/eurjchem.10.4.345-349.1898

المؤلفون: Picazo, Elias

مصطلحات موضوعية: Organic chemistry, Akuammiline Alkaloids, Benzyne, Fischer Indolization Reaction, Natural Products, Strictamine, Total Synthesis

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/5086z618

المؤلفون: Smith, Joel Michael

مصطلحات موضوعية: Organic chemistry, Akuammiline, Alkaloid, Picrinine, Total Synthesis

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6d93p334

المؤلفون: Peng Zou (275872), Hongjian Yang (448197), Jian Wei (802495), Taimin Wang (3856468), Hongbin Zhai (1457509)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Microbiology, Cell Biology, Genetics, Molecular Biology, Physiology, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Dauben, Picrinine, nickel-mediated reductive Heck reaction, methoxyaspidophylline, oxidation, acid-promoted oxo-bridge ring-opening, Scholarisine, core, synthesis features, aldehyde functionality, azabicyclic, carbonyl O-cyclization, Total Synthesis, furoindoline scaffold, picrinine-type akuammiline alkaloids

Relation: https://figshare.com/articles/dataset/Total_Synthesis_of_-Picrinine_-Scholarisine_C_and_-5-_-Methoxyaspidophylline/15368452

الاتاحة: https://doi.org/10.1021/acs.orglett.1c02393.s002

المؤلفون: Wang, Taimin, Duan, Xiaoguang, Zhao, Hua, Zhai, Shengxian, Tao, Cheng, Wang, Huifei, Li, Yun, Cheng, Bin, Zhai, Hongbin

المساهمون: Zhai, HB (reprint author), Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China., Zhai, HB (reprint author), Peking Univ, Sch Chem Biol & Biotechnol, Key Lab Chem Genom, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China., Zhai, HB (reprint author), Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China., Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China., Peking Univ, Sch Chem Biol & Biotechnol, Key Lab Chem Genom, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China., Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China.

المصدر: SCI

مصطلحات موضوعية: CONCISE TOTAL-SYNTHESIS, FORMAL TOTAL-SYNTHESIS, AKUAMMILINE ALKALOIDS, NITROGEN ASSISTANCE, GOLD CATALYSIS, ENOL ETHERS, CYCLIZATION, (+/-)-ASPIDOPHYLLINE, (+/-)-STRICTAMINE, (+)-SCHOLARISINE

Relation: ORGANIC LETTERS.2017,19(7),1650-1653.; 1908392; http://hdl.handle.net/20.500.11897/474064; WOS:000398985800040

الاتاحة: https://hdl.handle.net/20.500.11897/474064
https://doi.org/10.1021/acs.orglett.7b00448

المؤلفون: Eckermann, Ruben

مصطلحات موضوعية: akuammiline alkaloids, Dewey Decimal Classification::500 | Naturwissenschaften::540 | Chemie, Akuammilin Alkaloide, ddc:540, conformational analysis, Konformationsanalyse, total synthesis, Totalsynthese

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b179ef0d10f0a4937f3a0a51b755450
https://www.repo.uni-hannover.de/handle/123456789/8490

المؤلفون: Jieping Zhu, Rémi Andres, Qian Wang

مصطلحات موضوعية: Tryptamine, akuammiline alkaloids, construction, cyclization, Stereochemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, chemistry.chemical_compound, Colloid and Surface Chemistry, indole alkaloids, Pictet–Spengler reaction, arboridinine, Chemistry, Enantioselective synthesis, reagents, Regioselectivity, Total synthesis, General Chemistry, 0104 chemical sciences, (+/-)-strictamine, absolute stereochemical assignment, Stereoselectivity, Epimer, Enantiomer, formal total-synthesis, carbonyl-compounds

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e488aa76447be5b040560ee7dce48ef
https://infoscience.epfl.ch/record/280025