المؤلفون: Weinzierl, David, Waser, Mario

مصطلحات موضوعية: ammonium ylides, chiral auxiliaries, cyclophanes, epoxides, paracyclophanes, ylides

جغرافية الموضوع: UL:TN:OC

وصف الملف: text/html

العلاقة: vignette : https://epub.jku.at/titlepage/urn/urn:nbn:at:at-ubl:3-7673/128Test; urn:nbn:at:at-ubl:3-7673; https://resolver.obvsg.at/urn:nbn:at:at-ubl:3-7673Test; local:99146176269703331; system:AC16263309

الإتاحة: https://doi.org/10.1002/hlca.202100073Test
https://resolver.obvsg.at/urn:nbn:at:at-ubl:3-7673Test

المؤلفون: Voskressensky L.G., Vorobiev I.V., Borisova T.N., Varlamov A.V.

المصدر: Journal of Organic Chemistry

مصطلحات موضوعية: Acetylene, Ammonium compounds, Chemical activation, Chemical reactions, Chemical reactivity, Hydrocarbons, Microfluidics, Activated alkynes, American Chemical Society (ACS), Ammonium ylides, Chemical equations, Multistage process (MSP), Naphthyridine, Reactivity (Chemical), Synthesis (of chiral ionic liquids), Synthesis (chemical), alkyne derivative, ammonium derivative, benzo[b]pyrrolo[2,1 f][1.6]naphthyridine derivative, naphthyridine derivative, pyrrole derivative, article, carbon nuclear magnetic resonance, crystal structure, molecular stability, proton nuclear magnetic resonance, quantum yield, reaction analysis, synthesis, X ray diffraction

العلاقة: https://doi.org/10.1021/jo8003698Test; https://openrepository.ru/article?id=253519Test

الإتاحة: https://doi.org/10.1021/jo8003698Test
https://openrepository.ru/article?id=253519Test

المؤلفون: West, Thomas H., Spoehrle, Stéphanie S. M., Smith, Andrew D.

المصدر: West , T H , Spoehrle , S S M & Smith , A D 2017 , ' Isothiourea-catalysed chemo- and enantioselective [2,3]-sigmatropic rearrangements of N , N -diallyl allylic ammonium ylides ' , Tetrahedron , vol. 73 , no. 29 , pp. 4138-4149 . https://doi.org/10.1016/j.tet.2017.01.062Test

مصطلحات موضوعية: [2,3]-rearrangement, Isothiourea catalysis, Allylic ammonium ylides, Enantioselective catalysis, α-amino esters

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/isothioureacatalysed-chemo-and-enantioselective-23sigmatropic-rearrangements-of-nndiallyl-allylicTest-ammonium-ylides(ff39a291-b4c9-4ddc-9455-46f06d19a635).html

الإتاحة: https://doi.org/10.1016/j.tet.2017.01.062Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/isothioureacatalysed-chemo-and-enantioselective-23sigmatropic-rearrangements-of-nndiallyl-allylicTest-ammonium-ylides(ff39a291-b4c9-4ddc-9455-46f06d19a635).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/12636/1/Smith_2017_Tetrahedron_AmmoniumYlides_AAM.pdfTest
http://www.sciencedirect.com/science/article/pii/S0040402017300972#appd001Test

المؤلفون: Kasten, Kevin, Slawin, Alexandra M. Z., Smith, Andrew D.

المصدر: Kasten , K , Slawin , A M Z & Smith , A D 2017 , ' Enantioselective synthesis of β-fluoro-β-aryl-α-amino pentenamides by organocatalytic [2,3]-sigmatropic rearrangement ' , Organic Letters , vol. 19 , no. 19 , pp. 5182-5185 . https://doi.org/10.1021/acs.orglett.7b02452Test

مصطلحات موضوعية: Flluorinated amino-acids, Allylic ammonium ylides, Kinetic resolution, Medicinal chemistry, Protein design, Catalysts, Mannich, Benzotetramisole, Straightforward, Cycloaddition

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/enantioselective-synthesis-of-fluoroarylamino-pentenamides-by-organocatalytic-23sigmatropic-rearrangementTest(07670065-865e-41af-9c62-6aebd918224a).html

الإتاحة: https://doi.org/10.1021/acs.orglett.7b02452Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/enantioselective-synthesis-of-fluoroarylamino-pentenamides-by-organocatalytic-23sigmatropic-rearrangementTest(07670065-865e-41af-9c62-6aebd918224a).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/15992/1/Smith_2017_OrgLetters_Enantioselectve_AAM.pdfTest

المؤلفون: West, Thomas Henry, Spoehrle, Stephanie Suzanne Madeleine, Kasten, Kevin, Taylor, James Edward, Smith, Andrew David

المصدر: West , T H , Spoehrle , S S M , Kasten , K , Taylor , J E & Smith , A D 2015 , ' Catalytic stereoselective [2,3]-rearrangement reactions ' , ACS Catalysis , vol. In press . https://doi.org/10.1021/acscatal.5b02070Test

مصطلحات موضوعية: Stereoselective catalysis, [2,3]-rearrangement, Allylic oxonium ylides, Allylic ammonium ylides, O-propargylic oximes, Allylic sulfoxides, Allylic N-oxides

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/catalytic-stereoselective-23rearrangement-reactionsTest(a4851398-1b1a-4731-ae2d-a38bb03a5a21).html

الإتاحة: https://doi.org/10.1021/acscatal.5b02070Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/catalytic-stereoselective-23rearrangement-reactionsTest(a4851398-1b1a-4731-ae2d-a38bb03a5a21).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/9734/1/Smith_2015_ACSC_Catalytic_AM.pdfTest

المؤلفون: Kasten, Kevin, Slawin, Alexandra M. Z., Smith, Andrew D.

المساهمون: European Commission, The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: Flluorinated amino-acids, Allylic ammonium ylides, Kinetic resolution, Medicinal chemistry, Protein design, Catalysts, Mannich, Benzotetramisole, Straightforward, Cycloaddition, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Organic Letters; 250962719; 07670065-865e-41af-9c62-6aebd918224a; 000412789600045; 85032614861; Kasten , K , Slawin , A M Z & Smith , A D 2017 , ' Enantioselective synthesis of β-fluoro-β-aryl-α-amino pentenamides by organocatalytic [2,3]-sigmatropic rearrangement ' , Organic Letters , vol. 19 , no. 19 , pp. 5182-5185 . https://doi.org/10.1021/acs.orglett.7b02452Test; ORCID: /0000-0002-2104-7313/work/37255560; ORCID: /0000-0002-9527-6418/work/56861707; https://hdl.handle.net/10023/15992Test; N/A; WM140071

الإتاحة: https://doi.org/10.1021/acs.orglett.7b02452Test
https://hdl.handle.net/10023/15992Test

المؤلفون: West, Thomas H., Spoehrle, Stéphanie S. M., Smith, Andrew D.

المساهمون: European Commission, The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: [2,3]-rearrangement, Isothiourea catalysis, Allylic ammonium ylides, Enantioselective catalysis, α-amino esters, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Tetrahedron; 249036825; ff39a291-b4c9-4ddc-9455-46f06d19a635; 85013441087; 000405158400015; West , T H , Spoehrle , S S M & Smith , A D 2017 , ' Isothiourea-catalysed chemo- and enantioselective [2,3]-sigmatropic rearrangements of N , N -diallyl allylic ammonium ylides ' , Tetrahedron , vol. 73 , no. 29 , pp. 4138-4149 . https://doi.org/10.1016/j.tet.2017.01.062Test; RIS: urn:0E61E9C036C60511338C857E4F9FD3AF; ORCID: /0000-0002-2104-7313/work/36567476; https://hdl.handle.net/10023/12636Test; http://www.sciencedirect.com/science/article/pii/S0040402017300972#appd001Test; SUBICAT; WM140071; N/A

الإتاحة: https://doi.org/10.1016/j.tet.2017.01.062Test
https://hdl.handle.net/10023/12636Test
http://www.sciencedirect.com/science/article/pii/S0040402017300972#appd001Test

المؤلفون: Kevin Kasten, Andrew D. Smith, Alexandra M. Z. Slawin

المساهمون: European Commission, The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

المصدر: Organic letters. 19(19)

مصطلحات موضوعية: Allylic ammonium ylides, Stereochemistry, 2,3-sigmatropic rearrangement, Substituent, Medicinal chemistry, 010402 general chemistry, Straightforward, 01 natural sciences, Biochemistry, Stereocenter, Kinetic resolution, Benzotetramisole, chemistry.chemical_compound, Benzylamine, QD, Physical and Theoretical Chemistry, Cycloaddition, Catalysts, 010405 organic chemistry, Chemistry, Aryl, Organic Chemistry, Enantioselective synthesis, Mannich, DAS, QD Chemistry, 0104 chemical sciences, Protein design, Flluorinated amino-acids

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1240ead707ec1bc772a5fb1dedaf9313Test
https://pubmed.ncbi.nlm.nih.gov/28885031Test

المؤلفون: MIDYA, SP, GOPI, E, SATAM, N, NAMBOOTHIRI, INN

مصطلحات موضوعية: Containing Natural-Products, Highly Substituted Pyrroles, One-Pot, Efficient Synthesis, Ammonium Ylides, Organic-Synthesis, Organocatalytic Cyclopropanation, Enantioselective Synthesis, Polysubstituted Pyrroles, Functionalized Pyrroles

العلاقة: ORGANIC & BIOMOLECULAR CHEMISTRY,15(17)3616-3627; http://dx.doi.org/10.1039/c7ob00529fTest

الإتاحة: https://doi.org/10.1039/c7ob00529fTest

المؤلفون: Andrew D. Smith, Stephanie S. M. Spoehrle, Thomas H. West

المساهمون: European Commission, The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: Allylic rearrangement, Allylic ammonium ylides, 010405 organic chemistry, Organic Chemistry, Enantioselective synthesis, DAS, Sigmatropic reaction, [2,3]-rearrangement, 010402 general chemistry, QD Chemistry, 01 natural sciences, Biochemistry, Isothiourea catalysis, 0104 chemical sciences, chemistry.chemical_compound, chemistry, α-amino esters, Drug Discovery, Organic chemistry, Ammonium, QD, Piperidine, Enantioselective catalysis

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcea0117056f9510a74825ad9afb2dc7Test
http://www.sciencedirect.com/science/article/pii/S0040402017300972#appd001Test