المؤلفون: Chepuri V. Ramana

مصطلحات موضوعية: Rh[III] Catalysis, C-H activation, Cross dehydrogenative coupling, GBT-440, diazoester. TIPS-EBX

Relation: https://doi.org/10.5281/zenodo.7813199; https://doi.org/10.5281/zenodo.7813200; oai:zenodo.org:7813200

الاتاحة: https://doi.org/10.5281/zenodo.7813200

المؤلفون: Kexin Dong, Xun-Shen Liu, Xiaoyan Wei, Yuting Zhao, Lu Liu

المصدر: Green Synthesis and Catalysis, Vol 2, Iss 4, Pp 385-388 (2021)

مصطلحات موضوعية: Borane-catalysed, Diazoester, S–H insertion, Thiophenols, Thiols, C–S bond Formation, Chemical technology, TP1-1185, Biochemistry, QD415-436

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S266655492100082X; https://doaj.org/toc/2666-5549

URL الوصول: https://doaj.org/article/90d579aed92f4a18a153c93583bdb5b0

المؤلفون: Herman O. Sintim, Hamad H. Al Mamari, Hasanain A. A. Almohseni, Younes Fegheh-Hassanpour, David M. Hodgson

المصدر: Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 1194-1202 (2019)

مصطلحات موضوعية: alkylation, cycloaddition, diazoester, epimerisation, tartaric acid, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/efbda8b9d278435d89edc2c55e3d5be7

المؤلفون: Marcus, Jørgen

المصدر: Marcus, Jørgen. Reactivity of Halodiazoacetates and Halodiazoamides. Master thesis, University of Oslo, 2022

الاتاحة: http://hdl.handle.net/10852/95885
https://www.duo.uio.no/bitstream/handle/10852/95885/5/Master-Joergen.pdf

المؤلفون: Hamada S. A. Mandour, Yoko Nakagawa, Masaya Tone, Hayato Inoue, Nansalmaa Otog, Ikuhide Fujisawa, Soda Chanthamath, Seiji Iwasa

المصدر: Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 357-363 (2019)

مصطلحات موضوعية: asymmetric synthesis, carbene transfer, cyclopropanation, diazoester, intramolecular diazoamide, Ru(II)-Pheox, water-soluble catalyst, Weinreb amide, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/f47030cdedfd40c0bf91e708c5d46e5d

المؤلفون: Ayan Dasgupta, Emma Richards, Rebecca L. Melen

المصدر: ACS Catalysis

مصطلحات موضوعية: Perspective, triarylborane, General Chemistry, diazoester, Catalysis, carbene transfer, diazo activation

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e55de0571701a686f84f4edc0252fcf
https://doi.org/10.1021/acscatal.1c04746

المؤلفون: Alireza Ariafard, Ayan Dasgupta, Lukas Gierlichs, Rebecca L. Melen, Katarina Stefkova, Rasool Babaahmadi, Sanjukta Pahar, Brian F. Yates

المصدر: Angewandte Chemie (International Ed. in English)

مصطلحات موضوعية: carbenium, Reaction mechanism, Communication, Aryl, General Chemistry, Pyrazole, Borane, Combinatorial chemistry, Communications, Catalysis, pyrazole, Homogeneous Catalysis, chemistry.chemical_compound, Carbenium ion, chemistry, autocatalysis, aryl ester, Organic synthesis, Tris(pentafluorophenyl)borane, diazoester

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4bedf103d9d31257fa567e94777902b
https://doi.org/10.1002/anie.202109744

المؤلفون: László B. Balázs, Sumod A. Pullarkat, Yinhua Huang, Pak-Hing Leung, Yongxin Li, Jasmina Begam Khalikuzzaman

المساهمون: School of Physical and Mathematical Sciences

المصدر: The Journal of Organic Chemistry. 85:14763-14771

مصطلحات موضوعية: Diarylphosphine, Organic Chemistry, chemistry.chemical_element, Bond formation, Nitrogen, Medicinal chemistry, Stereocenter, Catalysis, chemistry.chemical_compound, Alpha Diazoester Derivative, chemistry, Chemistry [Science], Electrophile, Diazo, Derivatization, Carbene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606c6de514bddd1a77c2a05386bfad1d
https://doi.org/10.1021/acs.joc.0c00181

المؤلفون: Dasgupta, A, Pahar, S, Babaahmadi, R, Gierlichs, L, Yates, BF, Ariafard, A, Melen, RL

مصطلحات موضوعية: borane catalysis, DFT calculations, diazo compounds, diazoester, pyrazole, carbene, tris(pentafluorophenyl)borane, Density Functional Theory

وصف الملف: application/pdf

Relation: https://eprints.utas.edu.au/46600/1/150055%20-%20Borane%20catalyzed%20selective%20diazo%20cross-coupling.pdf; Dasgupta, A, Pahar, S, Babaahmadi, R, Gierlichs, L, Yates, BF orcid:0000-0001-9663-3301 , Ariafard, A orcid:0000-0003-2383-6380 and Melen, RL 2022 , 'Borane catalyzed selective diazo cross-coupling towards pyrazoles' , Advanced Synthesis and Catalysis, vol. 364, no. 4 , pp. 773-780 , doi: https://doi.org/10.1002/adsc.202101312 .

الاتاحة: https://eprints.utas.edu.au/46600/
https://eprints.utas.edu.au/46600/1/150055%20-%20Borane%20catalyzed%20selective%20diazo%20cross-coupling.pdf

المؤلفون: Nansalmaa Otog, Ikuhide Fujisawa, Masaya Tone, Seiji Iwasa, Soda Chanthamath, Hayato Inoue, Hamada S. A. Mandour, Yoko Nakagawa

المصدر: Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 357-363 (2019)

مصطلحات موضوعية: water-soluble catalyst, Letter, Ru(II)-Pheox, Cyclopropanation, asymmetric synthesis, cyclopropanation, Medicinal chemistry, Cyclopropane, Catalysis, carbene transfer, lcsh:QD241-441, chemistry.chemical_compound, lcsh:Organic chemistry, Amide, lcsh:Science, diazoester, Weinreb amide, Bicyclic molecule, Chemistry, Organic Chemistry, Enantioselective synthesis, Intramolecular force, intramolecular diazoamide, lcsh:Q, Diazo

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e29153915d8c134044941941a6a56c
http://europepmc.org/articles/PMC6369996

المؤلفون: Martín, Carmen, Molina González, Francisco, Álvarez, Eleuterio, Rodríguez Belderraín, Tomás

مصطلحات موضوعية: Diazoester, Cyclopropanation, Homogeneous catalysis, Palladium

Relation: info:eu-repo/grantAgreement/Ministerio de Ciencia e Innovacion [CTQ2008-00042BQU, CTQ2011-24502]; info:eu-repo/grantAgreement/Junta de Andalucia [P07-FQM-02794]; http://hdl.handle.net/10272/11567

الاتاحة: http://hdl.handle.net/10272/11567
https://doi.org/10.1002/chem.201102900

المؤلفون: Hamad H. Al Mamari, Hasanain A. A. Almohseni, David M. Hodgson, Younes Fegheh-Hassanpour, Herman O. Sintim

المصدر: Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 1194-1202 (2019)

مصطلحات موضوعية: Tartrate, Alkylation, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, Full Research Paper, lcsh:QD241-441, chemistry.chemical_compound, Deprotonation, lcsh:Organic chemistry, lcsh:Science, alkylation, diazoester, cycloaddition, epimerisation, Octane, chemistry.chemical_classification, 010405 organic chemistry, Organic Chemistry, Enantioselective synthesis, Diastereomer, 0104 chemical sciences, Chemistry, chemistry, tartaric acid, Ylide, Tartaric acid, lcsh:Q

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c2c0675839ad88f7f569629c12085d
https://ora.ox.ac.uk/objects/uuid:6ac7b66c-96fb-4ff9-a3c4-42a30e79d456

المؤلفون: Hisanori Nambu, Kazushi Minami, Masahiro Anada, Shunichi Hashimoto, 南 和志, 南部 寿則, 橋本 俊一, 穴田 仁洋

المصدر: Proceedings of the Symposium on Progress in Organic Reactions and Syntheses. 2005, :184

المؤلفون: Peter R. Norton, Keith Griffiths, Jason L. Pitters, Mark S. Workentin, Dana K. Adkinson

المصدر: Canadian Journal of Chemistry. 89:117-121

مصطلحات موضوعية: Diazoester, Photochemistry, Ketene, Surface reaction, Catalysis, Pt surfaces, chemistry.chemical_compound, Organic compounds, Monolayer, Single crystal surfaces, Electron energy levels, Reactivity (chemistry), Irradiation, Platinum, Monolayers, Photolysis, Organic Chemistry, Photodissociation, General Chemistry, chemistry, Carbenes, Saturated monolayers, Single crystal, Carbene, Surface reactions

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b6907d747dbdadf07e571d89751aa21
https://doi.org/10.1139/v10-113

المؤلفون: Montiege, Ophélie

المساهمون: Le Mans, Castanet, Anne-Sophie, Chany, Anne-Caroline

مصطلحات موضوعية: Chaxalactines, Synthèse totale, Macrolactone à 22 chaînons, Allénylation de Marshall, Couplage croisé, Diazoester, Insertion X-H, Acétal mixte monosilylé, Chaxalactins, Total synthesis, 22-membered macrolactone, Marshall allenylation, Cross coupling, X-H insertion, Monosilylated mixed acetal, 547.7, 547.2

Relation: http://www.theses.fr/2022LEMA1025

الاتاحة: http://www.theses.fr/2022LEMA1025

المؤلفون: 蕭萱霈, Hsiao, Hsuan-Pei

المساهمون: 吳學亮, Wu, Hsyueh-Liang

مصطلحات موضوعية: 一價銠金屬, 銠金屬碳烯中間體, 重氮酯類, 掌性雙環[2.2.2]雙烯配基, rhodium(I)-catalyzed, rhodiumcarbenoid, α-diazoester, chiral bicyclo [2.2.2] octadiene ligand

Relation: 60842048S-40033; https://etds.lib.ntnu.edu.tw/thesis/detail/e53379a477209678f8b067176a7779b9/; http://rportal.lib.ntnu.edu.tw/handle/20.500.12235/117234

الاتاحة: http://rportal.lib.ntnu.edu.tw/handle/20.500.12235/117234
https://hdl.handle.net/20.500.12235/117234
https://etds.lib.ntnu.edu.tw/thesis/detail/e53379a477209678f8b067176a7779b9/

المؤلفون: Stengel, Jason H.

المصدر: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1260473764.

مصطلحات موضوعية: Chemistry, Tandem reactions, diazoester, O-H insertion, Ring-closing metathesis, metallocarbenoid

Relation: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1260473764

الاتاحة: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1260473764

المؤلفون: Vanier, Sébastien F.

Thesis Advisors: Charette, André B.

مصطلحات موضوعية: hormaomycine, 3–(trans–2–aminocyclopropyl)alanine, bélactosine A, 3–(trans–2–nitrocyclopropyl)alanine, cyclopropanation stéréosélective intramoléculaire, réarrangement intramoléculaire, dérivés cyclopropaniques, synthèse formelle, diazoester, hormaomycin, belactosin A, diastereoselective intramolecular cyclopropanation reaction, intramolecular rearrangement, formal synthesis, aminocyclopropane, Chemistry - Organic / Chimie organique (UMI : 0490)

الاتاحة: http://hdl.handle.net/1866/3925

المؤلفون: 曲朝晖, 施卫峰, 金祥林, 王剑波

المساهمون: 北京大学化学学院, 生物有机与分子工程教育部重点实验室, 生物有机与分子工程教育部重点实验室 北京100871, 北京100871

المصدر: SCI ; 万方 ; 知网

مصطلحات موضوعية: 铑(II)卡宾, 重氮酰胺, 重氮酯, 构象分析, Rh(II) carbene, diazoamide, diazoester, conformational analysis

Relation: 有机化学.2003,(09),988-995+897.; 765517; http://hdl.handle.net/20.500.11897/78345; WOS:000188398900015

الاتاحة: https://hdl.handle.net/20.500.11897/78345
https://doi.org/10.3321/j.issn:0253-2786.2003.09.015

المؤلفون: 黃俊榮, Huang, Jun-Rong

المساهمون: 吳學亮, Wu, Hsyueh-Liang

مصطلحات موضوعية: 一價銠金屬, 掌性雙環雙烯配基, 不對稱加成反應, 憶思能, 共軛重氮酯類化合物, Rhodium (I), Bicyclo[2.2.1]chiral diene ligands, Asymmetric addition, Rivastigmine, Conjugate Diazoester

Relation: G060642075S; http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060642075S%22.&%22.id.&; http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100257

الاتاحة: http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100257
https://hdl.handle.net/20.500.12235/100257
http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060642075S%22.&%22.id.&