المؤلفون: Jiacheng Zhang (3597089), Xiaohong Huo (1830922), Junzhe Xiao (11236795), Ling Zhao (111365), Shengming Ma (1312428), Wanbin Zhang (1433917)

مصطلحات موضوعية: Microbiology, Molecular Biology, Ecology, Immunology, Developmental Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Central Chirality, acyclic systems, Diastereodivergent Construction, Pd, diastereoselective manner, allenylic esters, enantio, axial-to-central chirality transfer, nonadjacent stereocenters, diastereodivergent manner, representative transformations, chiral allenylic products, racemic allenylic esters

Relation: https://figshare.com/articles/journal_contribution/Enantio-_and_Diastereodivergent_Construction_of_1_3-Nonadjacent_Stereocenters_Bearing_Axial_and_Central_Chirality_through_Synergistic_Pd_Cu_Catalysis/15113344

الاتاحة: https://doi.org/10.1021/jacs.1c05087.s001

المؤلفون: Olivarès, Christel M.

مصطلحات موضوعية: 547, Fluorine, Amines, Hexafluoropropene, Acyclic systems, Cyclic systems

URL الوصول: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369317

المؤلفون: Beletskaya, Irina P., Nájera, Carmen, Yus, Miguel

المساهمون: Universidad de Alicante. Departamento de Química Orgánica, Síntesis Asimétrica (SINTAS)

مصطلحات موضوعية: Catalysis, Stereodivergence, Acyclic systems, Cyclic systems, Intramolecular cyclizations, Intermolecular cyclizations, Química Orgánica

Relation: https://doi.org/10.1021/acs.chemrev.7b00561; Chemical Reviews. 2018, 118(10): 5080-5200. doi:10.1021/acs.chemrev.7b00561; 0009-2665 (Print); 1520-6890 (Online); http://hdl.handle.net/10045/75951

الاتاحة: http://hdl.handle.net/10045/75951
https://doi.org/10.1021/acs.chemrev.7b00561

المؤلفون: Irina P. Beletskaya, Carmen Nájera, Miguel Yus

المساهمون: Universidad de Alicante. Departamento de Química Orgánica, Síntesis Asimétrica (SINTAS)

المصدر: RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)

مصطلحات موضوعية: Acyclic systems, Química Orgánica, Intermolecular cyclizations, 010405 organic chemistry, General Chemistry, 010402 general chemistry, Intramolecular cyclizations, 01 natural sciences, Catalysis, Stereodivergence, Cyclic systems, 0104 chemical sciences

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::597489d27bfc460862c9706b15b203eb
https://pubmed.ncbi.nlm.nih.gov/29676895

المؤلفون: Hiromitsu Maeda, Yohei Haketa, 前田 大光, 羽毛田 洋平

المصدر: Abstracts of Symposium on Physical Organic Chemistry. 2007, :16

المؤلفون: Hiromitsu Maeda, Yohei Haketa, 前田 大光, 羽毛田 洋平

المصدر: Abstracts of Symposium on Physical Organic Chemistry. 2007, :240

المؤلفون: Pierre-Olivier Delaye, Ilan Marek, Min Shi, Marwan Simaan

المساهمون: Technion - Israel Institute of Technology [Haifa], Infectiologie et Santé Publique (UMR ISP), Institut National de la Recherche Agronomique (INRA)-Université de Tours (UT), Chinese Academy of Sciences (CAS), Technion - Israel Institute of Technology, Institut National de la Recherche Agronomique (INRA)-Université de Tours

المصدر: Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2015, 54 (42), pp.12345-12348. ⟨10.1002/anie.201412440⟩

مصطلحات موضوعية: Stereochemistry, Metalation, [SDV]Life Sciences [q-bio], chemistry.chemical_element, metalation, Cyclopropene, STEREOGENIC CENTERS, 010402 general chemistry, Ring (chemistry), 01 natural sciences, Catalysis, Stereocenter, chemistry.chemical_compound, Cyclopropanol, Organic chemistry, small-ring systems, Quaternary carbon, 010405 organic chemistry, Chemistry, ETHYLMAGNESIUM BROMIDE, ENANTIOSELECTIVE CONSTRUCTION, General Medicine, ACYCLIC SYSTEMS, ORGANIC-SYNTHESIS, TRAXLER TRANSITION-STATE, General Chemistry, Copper, 0104 chemical sciences, 3. Good health, STEREOSELECTIVE-SYNTHESIS, DIASTEREOSELECTIVE SYNTHESIS, C-C BONDS, copper, strained molecules, synthetic methods, ALKYLMAGNESIUM HALIDES, Carbon

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::111910b33da6633c7435e9457bdce52b
https://doi.org/10.1002/anie.201412440

المؤلفون: Didier, Dorian, Delaye, Pierre-Olivier, Simaan, Marwan, Island, Biana, Eppe, Guillaume, Eijsberg, Hendrik, Kleiner, Amir, Knochel, Paul, Marek, Ilan

المساهمون: Technion - Israel Institute of Technology Haifa, Ludwig-Maximilians University Munich (LMU)

المصدر: ISSN: 0947-6539.

مصطلحات موضوعية: carbometalation, chelation, cyclopropene, diastereodivergence, QUATERNARY STEREOGENIC CENTERS, CARBONYL ALLYLATION REACTIONS, VERSATILE BUILDING-BLOCKS, RING STRAIN ENERGIES, ORGANOMAGNESIUM HALIDES, ACYCLIC SYSTEMS, C=C BONDS, ALKYLIDENECYCLOPROPANE DERIVATIVES, GRIGNARD-REAGENTS, INTRAMOLECULAR CARBOLITHIATION, copper, [SDV]Life Sciences [q-bio]

Relation: hal-02641468; https://hal.inrae.fr/hal-02641468; PRODINRA: 353777; WOS: 000329548000019

الاتاحة: https://hal.inrae.fr/hal-02641468
https://doi.org/10.1002/chem.201303569

المؤلفون: Ilan Marek, Amir Kleiner, Paul Knochel, Hendrik Eijsberg, Guillaume Eppe, Biana Island, Dorian Didier, Marwan Simaan, Pierre-Olivier Delaye

المساهمون: Technion - Israel Institute of Technology, Ludwig Maximilians University of Munich, Technion - Israel Institute of Technology [Haifa]

المصدر: Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (4), pp.1038-1048. ⟨10.1002/chem.201303569⟩

مصطلحات موضوعية: INTRAMOLECULAR CARBOLITHIATION, [SDV]Life Sciences [q-bio], ORGANOMAGNESIUM HALIDES, chemistry.chemical_element, Cyclopropene, VERSATILE BUILDING-BLOCKS, 010402 general chemistry, diastereodivergence, 01 natural sciences, Catalysis, Stereocenter, chemistry.chemical_compound, chelation, Fragmentation (mass spectrometry), Organic chemistry, Chelation, GRIGNARD-REAGENTS, Lewis acids and bases, 010405 organic chemistry, Organic Chemistry, Diastereomer, QUATERNARY STEREOGENIC CENTERS, ACYCLIC SYSTEMS, ALKYLIDENECYCLOPROPANE DERIVATIVES, General Chemistry, cyclopropene, Copper, 0104 chemical sciences, Carbometalation, chemistry, copper, C=C BONDS, CARBONYL ALLYLATION REACTIONS, RING STRAIN ENERGIES, carbometalation

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc78f7c2bf4c270fa970185cdcde8f89
https://pubmed.ncbi.nlm.nih.gov/24338953

المؤلفون: Yan, WG, Yeh, YN, Zhang, FJ, 张福基

المصدر: http://dx.doi.org/10.1002/qua.20688.

مصطلحات موضوعية: PI-ELECTRON ENERGY, HEXAGONAL CHAINS, LARGEST EIGENVALUE, PERFECT MATCHINGS, ACYCLIC SYSTEMS, HOSOYA INDEX, GRAPHS

Relation: International Journal of Quantum Chemistry, 2005,105(2):131-141; WOS:000232232200004; http://dspace.xmu.edu.cn/handle/2288/66261

الاتاحة: http://dspace.xmu.edu.cn/handle/2288/66261

المؤلفون: Hayes, Michael Patrick

المصدر: Chemistry - Dissertations

مصطلحات موضوعية: polypropionate-derived acyclic systems, streptovaricin D, Organic Chemistry

Relation: https://surface.syr.edu/che_etd/135; http://libezproxy.syr.edu/login?url=http://proquest.umi.com/pqdweb?did=736866121&sid=1&Fmt=2&clientId=3739&RQT=309&VName=PQD

الاتاحة: https://surface.syr.edu/che_etd/135
http://libezproxy.syr.edu/login?url=http://proquest.umi.com/pqdweb?did=736866121&sid=1&Fmt=2&clientId=3739&RQT=309&VName=PQD

المؤلفون: Dequeker, Elisabeth, Compernolle, Frans, Toppet, Suzanne, Hoornaert, Georges

مصطلحات موضوعية: acyclic systems, reduction, acids, derivatives, ketones, chirons

Relation: Tetrahedron vol:51 issue:20 pages:5877-5890; https://lirias.kuleuven.be/handle/123456789/33572; http://links.isiknowledge.com/Links/LinkOut.cgi?PID=ScienceDirect&source_PID=PRODUCT_NAME&origin=WOS_RETURN_URL&type=window&dest=http%3A%2F%2Fgateway.isiknowledge.com%2Fgateway%2FGateway.cgi%3FGWVersion%3D2%26SrcAuth%3DScienceDirect%26SrcApp%3DPRODUCT_NAME%26KeyAID%3D0040402095002395%26DestApp%3DScienceDirect%26SrcAppSID%3DAPP_SID%26SrcJTitle%3DWURS_TITLE

الاتاحة: https://lirias.kuleuven.be/handle/123456789/33572
http://links.isiknowledge.com/Links/LinkOut.cgi?PID=ScienceDirect&source_PID=PRODUCT_NAME&origin=WOS_RETURN_URL&type=window&dest=http%3A%2F%2Fgateway.isiknowledge.com%2Fgateway%2FGateway.cgi%3FGWVersion%3D2%26SrcAuth%3DScienceDirect%26SrcApp%3DPRODUCT_NAME%26KeyAID%3D0040402095002395%26DestApp%3DScienceDirect%26SrcAppSID%3DAPP_SID%26SrcJTitle%3DWURS_TITLE