المؤلفون: Bobing Tian, Jiahua Mao, Mingfu Zu, Ruilin Wu, Chao Xiao

مصطلحات موضوعية: Biophysics, Biochemistry, Physiology, Biotechnology, Developmental Biology, Cancer, Inorganic Chemistry, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, largest proportion causes, deprotonated hydroxy oxygen, covalent bond fracture, new xylose residue, density functional theory, alkali thermal pretreatment, four reaction paths, glycosidic bond oxygen, glycosidic bond breaks, nucleophile captures h30, lowest energy barrier, hemicellulose model compounds, glycosidic bond, energy barrier, glycoside bond, functional groups, alkali conditions, reaction path, reaction increases, ∼ 0

العلاقة: https://figshare.com/articles/journal_contribution/Study_of_the_Mechanism_of_Hydrolysis_of_Hemicellulose_from_Lignocellulose_during_Alkali_Thermal_Pretreatment_by_Density_Functional_Theory_and_Experiment/24964784Test

الإتاحة: https://doi.org/10.1021/acs.joc.3c01668.s001Test
https://figshare.com/articles/journal_contribution/Study_of_the_Mechanism_of_Hydrolysis_of_Hemicellulose_from_Lignocellulose_during_Alkali_Thermal_Pretreatment_by_Density_Functional_Theory_and_Experiment/24964784Test

المؤلفون: Paul V. Murphy, Ciaran O'Reilly, Wayne Pilgrim

المصدر: Molecules, Vol 18, Iss 9, Pp 11198-11218 (2013)

مصطلحات موضوعية: α-GalCer, anomerisation, glucuronic acid, galacturonic acid, glycoside bond, antigens, NKT cells, Organic chemistry, QD241-441

وصف الملف: electronic resource

العلاقة: http://www.mdpi.com/1420-3049/18/9/11198Test; https://doaj.org/toc/1420-3049Test

الوصول الحر: https://doaj.org/article/8a30220f76a04bb79c6328351b53bf25Test

المؤلفون: Pilgrim, Wayne, O'Reilly, Ciaran, Murphy, Paul

مصطلحات موضوعية: alpha-galcer, anomerisation, glucuronic acid, galacturonic acid, glycoside bond, antigens, nkt cells, killer t-cells, glucuronic-acid, glycosides, glycolipids, bacterial, analogs, recognition, infections, vaccines

العلاقة: Molecules; Pilgrim, Wayne; O'Reilly, Ciaran; Murphy, Paul (2013). Synthesis of a-o- and a-s-glycosphingolipids related to sphingomonous cell wall antigens using anomerisation. Molecules 18 (9), 11198-11218; http://hdl.handle.net/10379/13481Test

الإتاحة: https://doi.org/10.3390/molecules180911198Test
http://hdl.handle.net/10379/13481Test

المؤلفون: Wayne Pilgrim, Ciaran O'Reilly, Paul Murphy

المصدر: Molecules; Volume 18; Issue 9; Pages: 11198-11218

مصطلحات موضوعية: α-GalCer, anomerisation, glucuronic acid, galacturonic acid, glycoside bond, antigens, NKT cells

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: https://dx.doi.org/10.3390/molecules180911198Test

الإتاحة: https://doi.org/10.3390/molecules180911198Test

المؤلفون: Wayne Pilgrim, Paul V. Murphy

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.mdpi.com/1420-3049/18/9/11198/pdfTest/.

مصطلحات موضوعية: α-GalCer, anomerisation, glucuronic acid, galacturonic acid, glycoside bond

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.404.5981Test; http://www.mdpi.com/1420-3049/18/9/11198/pdfTest/

الإتاحة: http://www.mdpi.com/1420-3049/18/9/11198/pdfTest/

المؤلفون: Yasukazu OHKATSU

المصدر: Journal of Japan Oil Chemists' Society. 1996, 45(1):3

المؤلفون: Kim, Mijin, Kang, Soyeong, Rhee, Young Ho

المساهمون: Rhee, Young Ho

مصطلحات موضوعية: RING-CLOSING METATHESIS, GLYCOSIDE-BOND FORMATION, ALLYLIC ETHERIFICATION, CONSTRUCTION, DERIVATIVES, EFFICIENT, STRATEGY, AMINES, asymmetric synthesis, carbohydrates, de novo synthesis, diastereoselectivity, oligosaccharides

العلاقة: Angewandte chemie internatial edition; Chemistry, Multidisciplinary; Chemistry; https://oasis.postech.ac.kr/handle/2014.oak/37963Test; 19255; Angewandte chemie internatial edition, v.55, no.33, pp.9733 - 9737; 000383372700051; 2-s2.0-84982690179

الإتاحة: https://doi.org/10.1002/ANIE.201604199Test
https://oasis.postech.ac.kr/handle/2014.oak/37963Test

المؤلفون: Yang, Lin, Qin, Qi, Ye, Xin-Shan

المساهمون: Ye, XS (reprint author), Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China., Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China., Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China.

المصدر: SCI

مصطلحات موضوعية: carbohydrates, glycosylation, oligosaccharide synthesis, preactivation, stereoselectivity, 4,6-O-BENZYLIDENE-DIRECTED BETA-MANNOPYRANOSYLATION, NEIGHBORING-GROUP PARTICIPATION, DIRECT CHEMICAL-SYNTHESIS, ONE-POT SYNTHESIS, ANTIGEN GLOBO-H, ALPHA-SELECTIVE GLYCOSYLATIONS, HEPARAN-SULFATE PROTEOGLYCANS, GLYCOSIDE-BOND FORMATION, PRE-ACTIVATION PROTOCOL, 1,2-CIS O-GLYCOSYLATION

العلاقة: ASIAN JOURNAL OF ORGANIC CHEMISTRY.2013,2,(1),30-49.; 843813; http://hdl.handle.net/20.500.11897/157043Test; WOS:000325949000002

الإتاحة: https://doi.org/20.500.11897/157043Test
https://doi.org/10.1002/ajoc.201200136Test
https://hdl.handle.net/20.500.11897/157043Test

المؤلفون: Balmond, Edward I., Galan, M. Carmen, McGarrigle, Eoghan M.

المصدر: Balmond , E I , Galan , M C & McGarrigle , E M 2013 , ' Recent Developments in the Application of Organocatalysis to Glycosylations ' , SYNLETT , vol. 24 , no. 18 , ST-2013-P0452-SP , pp. 2335-2339 . https://doi.org/10.1055/s-0033-1338970Test

مصطلحات موضوعية: /dk/atira/pure/core/keywords/bcs_tecs_cdts, BCS and TECS CDTs, glycosylation, catalysis, organocatalysis, stereoselective synthesis, carbohydrates, regioselective synthesis, GLYCOSIDE-BOND FORMATION, ACID-BASE CATALYSIS, STEREOSELECTIVE GLYCOSYLATIONS, CARBOHYDRATE-DERIVATIVES, UREA ACTIVATION, SPIROKETALIZATIONS, OLIGOSACCHARIDE, IONS

الإتاحة: https://doi.org/10.1055/s-0033-1338970Test
https://hdl.handle.net/1983/ff2564fb-51bb-403b-a50e-364659b8b06aTest
https://research-information.bris.ac.uk/en/publications/ff2564fb-51bb-403b-a50e-364659b8b06aTest
http://www.scopus.com/inward/record.url?scp=84881301343&partnerID=8YFLogxKTest

المؤلفون: Geng, Yiqun, Qin, Qi, Ye, Xin-Shan

المساهمون: Ye, XS (reprint author), Peking Univ, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China., Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China., Peking Univ, Sch Pharmaceut Sci, Beijing 100191, Peoples R China., Peking Univ, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China.

المصدر: EI ; PubMed ; SCI

مصطلحات موضوعية: CARBOHYDRATE BENZYLIDENE ACETALS, GLYCOSIDE-BOND FORMATION, PRE-ACTIVATION PROTOCOL, ONE-POT SYNTHESIS, OLIGOSACCHARIDE SYNTHESIS, STEREOSELECTIVE GLYCOSYLATIONS, CHEMOSELECTIVE GLYCOSYLATIONS, BETA-MANNOPYRANOSIDES, ENDOCYCLIC CLEAVAGE, PROTECTING GROUPS

العلاقة: JOURNAL OF ORGANIC CHEMISTRY.2012,77,(12),5255-5270.; 660573; http://hdl.handle.net/20.500.11897/192259Test; WOS:000305205400005

الإتاحة: https://doi.org/20.500.11897/192259Test
https://doi.org/10.1021/jo3002084Test
https://hdl.handle.net/20.500.11897/192259Test