المؤلفون: Abhijit Sau, Anup Kumar Misra

المصدر: Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 2053-2059 (2012)

مصطلحات موضوعية: Escherichia coli, glycosylation, lipopolysaccharide, O-antigen, tetrasaccharide, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/d35530754bb248f392bdd9a36c2c31e5

المؤلفون: Abhijit Sau, Anup Kumar Misra

المصدر: PLoS ONE, Vol 7, Iss 5, p e37291 (2012)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3360696?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/7b2a0558952e45969fe34bef07692c38

المؤلفون: Abhijit Sau, Daria Brykczyńska, Joseph Moran, Christopher N. Rowley, Paul Chatelain, Cyprien Muller, Maryam Bahadori

المساهمون: Institut de Science et d'ingénierie supramoléculaires (ISIS), Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et Nanosciences Grand-Est (MNGE), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Adam Mickiewicz University in Poznań (UAM), Carleton University, ANR-10-IDEX-0002,UNISTRA,Par-delà les frontières, l'Université de Strasbourg(2010), European Project: 792101,VSC_CAT, Réseau nanophotonique et optique, Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA), univOAK, Archive ouverte

المصدر: Angewandte Chemie International Edition
Angewandte Chemie International Edition, 2021, 60 (48), pp.25307-25312. ⟨10.1002/anie.202111977⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (48), pp.25307-25312. ⟨10.1002/anie.202111977⟩

مصطلحات موضوعية: Sulfonyl, chemistry.chemical_classification, 010405 organic chemistry, Chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Aryl, [CHIM.CATA] Chemical Sciences/Catalysis, General Medicine, General Chemistry, [CHIM.CATA]Chemical Sciences/Catalysis, [CHIM.ORGA] Chemical Sciences/Organic chemistry, 010402 general chemistry, 01 natural sciences, Oxidative addition, Combinatorial chemistry, Catalysis, 0104 chemical sciences, chemistry.chemical_compound, Transmetalation, Suzuki reaction, Electrophile, Reactivity (chemistry)

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::486d02ed665260c8a0bb266a813acf9b
https://hal.science/hal-03468102

المؤلفون: Abhijit Sau, M. Carmen Galan

المصدر: Organic Letters
Sau, A & Galan, M C 2017, ' Palladium-Catalyzed α-Stereoselective O-Glycosylation of O(3)-Acylated Glycals ', Organic Letters, vol. 19, no. 11, pp. 2857-2860 . https://doi.org/10.1021/acs.orglett.7b01092

مصطلحات موضوعية: chemistry.chemical_classification, Glycosylation, Letter, 010405 organic chemistry, Stereochemistry, Glycoconjugate, Organic Chemistry, chemistry.chemical_element, Glycoside, Alcohol, 010402 general chemistry, 01 natural sciences, Biochemistry, Medicinal chemistry, 0104 chemical sciences, Catalysis, chemistry.chemical_compound, chemistry, Nucleophile, Stereoselectivity, Physical and Theoretical Chemistry, Palladium

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c98698d5fb2ba09d1573b5e6c8f1a1b
http://europepmc.org/articles/PMC5479629

المؤلفون: M. Carmen Galan, Helene Ledru, Abhijit Sau, Mattia Ghirardello

المصدر: Ghirardello, M, Ledru, H, Sau, A & Galan, M C 2020, ' Chemo-selective Rh-catalysed hydrogenation of azides into amines ', Carbohydrate Research, vol. 489, pp. 107948 . https://doi.org/10.1016/j.carres.2020.107948
Carbohydrate Research

مصطلحات موضوعية: Azides, High selectivity, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, Analytical Chemistry, chemistry.chemical_compound, Hydrogenolysis, Chemo-selective reduction, Carbohydrate Conformation, Organic chemistry, Rhodium, Amines, Rhodium catalysis, Catalytic hydrogenation, chemistry.chemical_classification, 010405 organic chemistry, Chemistry, Organic Chemistry, Azide reduction, General Medicine, Carbohydrate, 0104 chemical sciences, Amino acid, Protecting groups manipulation, Aminoglycosides, Azide, Hydrogenation

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::236632cf68481a76742135ab85797932
https://hdl.handle.net/1983/5dd699fa-02ce-45fe-8b01-0e2bc607db40

المؤلفون: Abhijit Sau, M. Carmen Galan, Maristela Braga Martins-Teixeira, Carlos Palo-Nieto, Laurence Grimaud, Robin Jeanneret, Pierre-Adrien Payard, Ivone Carvalho, Aude Salamé

المساهمون: University of Bristol [Bristol], Laboratoire des biomolécules (LBM UMR 7203), Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Département de Chimie - ENS Paris, École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Chimie Moléculaire de Paris Centre (FR 2769), Institut de Chimie du CNRS (INC)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of São Paulo (USP), Chimie Moléculaire de Paris Centre (FR 2769), École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Département de Chimie - ENS Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Universidade de São Paulo = University of São Paulo (USP), Gestionnaire, Hal Sorbonne Université

المصدر: Organic Letters
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Organic Letters, American Chemical Society, 2020, 22 (5), pp.1991-1996. ⟨10.1021/acs.orglett.9b04525⟩
Organic Letters, 2020, 22 (5), pp.1991-1996. ⟨10.1021/acs.orglett.9b04525⟩

مصطلحات موضوعية: Glycosylation, CARBOIDRATOS, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, chemistry.chemical_compound, Nucleophile, Oxidation state, Reactivity (chemistry), Glycosides, Physical and Theoretical Chemistry, chemistry.chemical_classification, Molecular Structure, 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, [CHIM.CATA] Chemical Sciences/Catalysis, [CHIM.CATA]Chemical Sciences/Catalysis, [CHIM.ORGA] Chemical Sciences/Organic chemistry, Combinatorial chemistry, 0104 chemical sciences, 3. Good health, chemistry, Enol ether, Stereoselectivity, Counterion, Oxidation-Reduction, Copper

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f7ae0a8f9eb5b9cde72a2cdaadad6b5

المؤلفون: Abhijit Sau, Ivone Carvalho, Robin Jeanneret, M. Carmen Galan, Carlos Palo-Nieto, Pierre-Adrien Payard, Laurence Grimaud, Maristela Braga Martins-Teixeira

مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, Glycosylation, chemistry, Nucleophile, Oxidation state, Enol ether, Stereoselectivity, Reactivity (chemistry), Counterion, Combinatorial chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99d318b0b43f5abbeed274f64b0ca4ee
https://doi.org/10.26434/chemrxiv.9272684

المؤلفون: Christopher N. Rowley, Paul Chatelain, Abhijit Sau, Joseph Moran

مصطلحات موضوعية: Coupling (electronics), chemistry.chemical_compound, chemistry, Aryl, Electrophile, Nitro, chemistry.chemical_element, Halide, Medicinal chemistry, Oxidative addition, Sulfone, Palladium

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c7e817a8bf93e82935353ac93110257
https://doi.org/10.26434/chemrxiv.8083028

المؤلفون: Ryan Williams, Carlos Palo-Nieto, Sandra Medina, M. Carmen Galan, Abhijit Sau, Antonio Franconetti

المصدر: Angewandte Chemie International Edition
Angewandte Chemie (International Ed. in English)
Sau, A, Williams, R, Palo Nieto, C, Franconetti Garcia, A, Medina Villar, S & Galan, C 2017, ' Palladium-catalysed direct stereoselective synthesis of deoxyglycosides from glycals ', Angewandte Chemie-International Edition, vol. 56, no. 13, pp. 3640–3644 . https://doi.org/10.1002/anie.201612071

مصطلحات موضوعية: Denticity, glycosylation, Glycal, chemistry.chemical_element, 010402 general chemistry, acetals, 01 natural sciences, Catalysis, chemistry.chemical_compound, Nucleophile, Organic chemistry, chemistry.chemical_classification, deoxyglycosides, 010405 organic chemistry, Alkene, Communication, asymmetric catalysis, General Medicine, General Chemistry, palladium, Combinatorial chemistry, Communications, 0104 chemical sciences, Homogeneous Catalysis, chemistry, Alkoxy group, Phosphine, Palladium

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b739b3d176d45d70cc39df5ccdb033
https://doi.org/10.1002/anie.201612071

المؤلفون: Abhijit, Sau, Carlos, Palo-Nieto, M Carmen, Galan

المصدر: The Journal of organic chemistry. 84(5)

مصطلحات موضوعية: Glycosylation, Hydrocarbons, Fluorinated, Ethers, Cyclic, Stereoisomerism, Glycosides, Boranes, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d57ae945a64e079b993819a64d021090
https://pubmed.ncbi.nlm.nih.gov/30706711

المؤلفون: M. Carmen Galan, Abhijit Sau, Carlos Palo-Nieto

المصدر: Sau, A, Palo-Nieto, C & Galan, M C 2019, ' Substrate-Controlled Direct α-Stereoselective Synthesis of Deoxyglycosides from Glycals Using B(C 6 F 5 ) 3 as Catalyst ', Journal of Organic Chemistry, vol. 84, no. 5, pp. 2415-2424 . https://doi.org/10.1021/acs.joc.8b02613
The Journal of Organic Chemistry

مصطلحات موضوعية: Organisk kemi, 010405 organic chemistry, Chemistry, Organic Chemistry, Substrate (chemistry), Stereoselectivity, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, 0104 chemical sciences, Catalysis

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79af1cf099b65ec86616dd77ab38cac6
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-461459

المؤلفون: Abhijit Sau, Joseph Moran, Christopher N. Rowley, Paul Chatelain

المساهمون: Institut de Science et d'ingénierie supramoléculaires (ISIS), Université Louis Pasteur - Strasbourg I-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Réseau nanophotonique et optique, Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)

المصدر: Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2019, 58 (42), pp.14959-14963. ⟨10.1002/anie.201908336⟩
Angewandte Chemie

مصطلحات موضوعية: 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Aryl, General Chemistry, General Medicine, 010402 general chemistry, Combinatorial chemistry, Oxidative addition, 01 natural sciences, Catalysis, Sulfone, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Coupling (computer programming), Electrophile, Functional group, Nitro, Reactivity (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::524682adeac3c92c3b01cf09c2481b5c

المؤلفون: Reko Leino, Abhijit Sau, Anssi Peuronen, Andreas Gunell, Tiina Saloranta-Simell, Ida Mattsson, Manu Lahtinen

مصطلحات موضوعية: Diffraction, Materials science, 010402 general chemistry, 01 natural sciences, Differential scanning calorimetry, NMR spectroscopy, crystals, General Materials Science, kalorimetria, NMR-spektroskopia, ta116, x-ray crystallography, Aqueous solution, 010405 organic chemistry, Diastereomer, General Chemistry, Condensed Matter Physics, kiteet, 0104 chemical sciences, sokerialkoholit, Crystallography, sugar alcohols, Polymorphism (materials science), Melting point, Enantiomer, Single crystal, calorimetry, röntgenkristallografia

وصف الملف: application/pdf; fulltext

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ab96a7a9f86a934060b33c8d8cb0fcd
http://urn.fi/URN:NBN:fi:jyu-202006234362

المؤلفون: Anup Kumar Misra, Manas Jana, Abhijit Sau

المصدر: Tetrahedron: Asymmetry. 25:632-636

مصطلحات موضوعية: chemistry.chemical_classification, animal structures, Tetrafluoroborate, Glycosylation, Strain (chemistry), Activator (genetics), Stereochemistry, Organic Chemistry, macromolecular substances, Polysaccharide, Catalysis, carbohydrates (lipids), Inorganic Chemistry, Cell wall, chemistry.chemical_compound, chemistry, Antigen, lipids (amino acids, peptides, and proteins), Glycosyl, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::45fccd7b446156c5652f0673a759c2da
https://doi.org/10.1016/j.tetasy.2014.03.007

المؤلفون: Abhijit Sau, Anup Kumar Misra, Debashis Dhara

المصدر: Tetrahedron: Asymmetry. 24:942-946

مصطلحات موضوعية: Glycosylation, Stereochemistry, Organic Chemistry, medicine.disease_cause, Combinatorial chemistry, High yielding, Catalysis, carbohydrates (lipids), Inorganic Chemistry, chemistry.chemical_compound, chemistry, Antigen, medicine, lipids (amino acids, peptides, and proteins), Stereoselectivity, Physical and Theoretical Chemistry, Escherichia coli

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8f538b2bdc11a44c085d9a43ff34ec61
https://doi.org/10.1016/j.tetasy.2013.06.005

المؤلفون: Anup Kumar Misra, Abhijit Sau

المصدر: Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 2053-2059 (2012)

مصطلحات موضوعية: animal structures, Anomer, Glycosylation, glycosylation, Stereochemistry, tetrasaccharide, Disaccharide, Convergent synthesis, macromolecular substances, medicine.disease_cause, Full Research Paper, lcsh:QD241-441, chemistry.chemical_compound, lcsh:Organic chemistry, medicine, Escherichia coli, Tetrasaccharide, lcsh:Science, Protecting group, Organic Chemistry, lipopolysaccharide, O-antigen, carbohydrates (lipids), Chemistry, chemistry, Biochemistry, lcsh:Q, lipids (amino acids, peptides, and proteins), Linker

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6627f6938ae2cf4f2ec37b3c52c3769d
http://europepmc.org/articles/PMC3511039

المؤلفون: Anup Kumar Misra, Abhijit Sau

المصدر: Carbohydrate Research. 361:41-48

مصطلحات موضوعية: chemistry.chemical_classification, Glycal, education, Organic Chemistry, Disaccharide, Glycoside, General Medicine, Biochemistry, Analytical Chemistry, chemistry.chemical_compound, chemistry, Alcohols, Organoselenium Compounds, Yield (chemistry), Benzene Derivatives, Carbohydrate Conformation, Organic chemistry, Bromosuccinimide, Glycosyl, Glycosides, N-Bromosuccinimide, Alkyl

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd1375ae31e1cbfd29897853a9b3c946
https://doi.org/10.1016/j.carres.2012.08.009

المؤلفون: Abhijit Sau, Abhishek Santra, Anup Kumar Misra

المصدر: Synlett. 23:2341-2348

مصطلحات موضوعية: chemistry.chemical_classification, animal structures, Tetrafluoroborate, Glycosylation, Stereochemistry, Organic Chemistry, Disaccharide, macromolecular substances, Oligosaccharide, Chemical synthesis, Catalysis, carbohydrates (lipids), chemistry.chemical_compound, chemistry, lipids (amino acids, peptides, and proteins), Glycosyl, Stereoselectivity

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a32273dc0eeaa865005b29d03969a50c
https://doi.org/10.1055/s-0032-1317135

المؤلفون: Abhijit Sau, Rajib Panchadhayee, Anup Kumar Misra, Debjani Ghosh

المصدر: Carbohydrate Research. 352:18-22

مصطلحات موضوعية: Glycosylation, Stereochemistry, Molecular Sequence Data, Disaccharide, Convergent synthesis, Oligosaccharides, Chemistry Techniques, Synthetic, Polysaccharide, Biochemistry, Analytical Chemistry, chemistry.chemical_compound, Tetrasaccharide, Reactivity (chemistry), chemistry.chemical_classification, biology, Organic Chemistry, O Antigens, Salmonella enterica, Stereoisomerism, General Medicine, biology.organism_classification, Carbohydrate Sequence, chemistry, Stereoselectivity

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ecc2eceb03f3bf077a7eb31ecbf3e1b
https://doi.org/10.1016/j.carres.2012.01.026

المؤلفون: Abhijit Sau, Anup Kumar Misra

المصدر: Synlett. 2011:1905-1911

مصطلحات موضوعية: Chemistry, Organic Chemistry, Thio, Environmentally friendly, Catalysis, Diselenide, Metal, chemistry.chemical_compound, visual_art, Ionic liquid, visual_art.visual_art_medium, Organic chemistry, Glycosyl, Triethylsilane

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a1cb85802c894a16b4bd2f0816ac6960
https://doi.org/10.1055/s-0030-1260966