Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis
Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6...
Ausführliche Beschreibung
Autor*in: |
Mereyala, Hari Babu [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
1994 |
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Schlagwörter: |
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Anmerkung: |
© Indian Academy of Sciences 1994 |
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Übergeordnetes Werk: |
Enthalten in: Proceedings of the Indian Academy of Sciences - Chemical Sciences - Springer India, 1980, 106(1994), 5 vom: Okt., Seite 1225-1230 |
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Übergeordnetes Werk: |
volume:106 ; year:1994 ; number:5 ; month:10 ; pages:1225-1230 |
Links: |
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DOI / URN: |
10.1007/BF02841929 |
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Katalog-ID: |
OLC2102744566 |
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10.1007/BF02841929 doi (DE-627)OLC2102744566 (DE-He213)BF02841929-p DE-627 ger DE-627 rakwb eng 000 500 060 VZ Mereyala, Hari Babu verfasserin aut Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis 1994 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Indian Academy of Sciences 1994 Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. Stereospecific mannosylations -inositol Mycobacterium tuberculosis Gaddam, Bapu Reddy aut Enthalten in Proceedings of the Indian Academy of Sciences - Chemical Sciences Springer India, 1980 106(1994), 5 vom: Okt., Seite 1225-1230 (DE-627)129381594 (DE-600)165276-X (DE-576)014766493 0370-0089 nnns volume:106 year:1994 number:5 month:10 pages:1225-1230 https://doi.org/10.1007/BF02841929 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-CHE SSG-OLC-MAT GBV_ILN_11 GBV_ILN_24 GBV_ILN_40 GBV_ILN_70 GBV_ILN_171 GBV_ILN_179 GBV_ILN_2003 GBV_ILN_2015 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4082 AR 106 1994 5 10 1225-1230 |
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10.1007/BF02841929 doi (DE-627)OLC2102744566 (DE-He213)BF02841929-p DE-627 ger DE-627 rakwb eng 000 500 060 VZ Mereyala, Hari Babu verfasserin aut Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis 1994 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Indian Academy of Sciences 1994 Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. Stereospecific mannosylations -inositol Mycobacterium tuberculosis Gaddam, Bapu Reddy aut Enthalten in Proceedings of the Indian Academy of Sciences - Chemical Sciences Springer India, 1980 106(1994), 5 vom: Okt., Seite 1225-1230 (DE-627)129381594 (DE-600)165276-X (DE-576)014766493 0370-0089 nnns volume:106 year:1994 number:5 month:10 pages:1225-1230 https://doi.org/10.1007/BF02841929 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-CHE SSG-OLC-MAT GBV_ILN_11 GBV_ILN_24 GBV_ILN_40 GBV_ILN_70 GBV_ILN_171 GBV_ILN_179 GBV_ILN_2003 GBV_ILN_2015 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4082 AR 106 1994 5 10 1225-1230 |
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10.1007/BF02841929 doi (DE-627)OLC2102744566 (DE-He213)BF02841929-p DE-627 ger DE-627 rakwb eng 000 500 060 VZ Mereyala, Hari Babu verfasserin aut Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis 1994 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Indian Academy of Sciences 1994 Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. Stereospecific mannosylations -inositol Mycobacterium tuberculosis Gaddam, Bapu Reddy aut Enthalten in Proceedings of the Indian Academy of Sciences - Chemical Sciences Springer India, 1980 106(1994), 5 vom: Okt., Seite 1225-1230 (DE-627)129381594 (DE-600)165276-X (DE-576)014766493 0370-0089 nnns volume:106 year:1994 number:5 month:10 pages:1225-1230 https://doi.org/10.1007/BF02841929 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-CHE SSG-OLC-MAT GBV_ILN_11 GBV_ILN_24 GBV_ILN_40 GBV_ILN_70 GBV_ILN_171 GBV_ILN_179 GBV_ILN_2003 GBV_ILN_2015 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4082 AR 106 1994 5 10 1225-1230 |
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10.1007/BF02841929 doi (DE-627)OLC2102744566 (DE-He213)BF02841929-p DE-627 ger DE-627 rakwb eng 000 500 060 VZ Mereyala, Hari Babu verfasserin aut Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis 1994 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Indian Academy of Sciences 1994 Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. Stereospecific mannosylations -inositol Mycobacterium tuberculosis Gaddam, Bapu Reddy aut Enthalten in Proceedings of the Indian Academy of Sciences - Chemical Sciences Springer India, 1980 106(1994), 5 vom: Okt., Seite 1225-1230 (DE-627)129381594 (DE-600)165276-X (DE-576)014766493 0370-0089 nnns volume:106 year:1994 number:5 month:10 pages:1225-1230 https://doi.org/10.1007/BF02841929 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-CHE SSG-OLC-MAT GBV_ILN_11 GBV_ILN_24 GBV_ILN_40 GBV_ILN_70 GBV_ILN_171 GBV_ILN_179 GBV_ILN_2003 GBV_ILN_2015 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4082 AR 106 1994 5 10 1225-1230 |
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10.1007/BF02841929 doi (DE-627)OLC2102744566 (DE-He213)BF02841929-p DE-627 ger DE-627 rakwb eng 000 500 060 VZ Mereyala, Hari Babu verfasserin aut Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis 1994 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Indian Academy of Sciences 1994 Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. Stereospecific mannosylations -inositol Mycobacterium tuberculosis Gaddam, Bapu Reddy aut Enthalten in Proceedings of the Indian Academy of Sciences - Chemical Sciences Springer India, 1980 106(1994), 5 vom: Okt., Seite 1225-1230 (DE-627)129381594 (DE-600)165276-X (DE-576)014766493 0370-0089 nnns volume:106 year:1994 number:5 month:10 pages:1225-1230 https://doi.org/10.1007/BF02841929 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-CHE SSG-OLC-MAT GBV_ILN_11 GBV_ILN_24 GBV_ILN_40 GBV_ILN_70 GBV_ILN_171 GBV_ILN_179 GBV_ILN_2003 GBV_ILN_2015 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4082 AR 106 1994 5 10 1225-1230 |
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Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis |
abstract |
Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. © Indian Academy of Sciences 1994 |
abstractGer |
Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. © Indian Academy of Sciences 1994 |
abstract_unstemmed |
Abstract Methyl iodide activated stereospecific α-mannosylations utilising 2-pyridyl-1-thiomannopyranoside derivatives (2,3,4) as donors and suitably protected myo-inositol derivatives (1,25,27,29) as acceptors to prepare 2-0-α-D-mannopyranosyl-6-[O-α-D-mannopyranosyl-(1–6)-O-α-D-mannopyranosyl-(l-6)-O-α-D-mannopyranosyl]-D-myo-inositol derivative (31) is described. © Indian Academy of Sciences 1994 |
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title_short |
Stereospecific mannosylations ofmyo-inasitol: Synthesis of manno-myo-inositol fragment ofMycobacterium tuberculosis |
url |
https://doi.org/10.1007/BF02841929 |
remote_bool |
false |
author2 |
Gaddam, Bapu Reddy |
author2Str |
Gaddam, Bapu Reddy |
ppnlink |
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isOA_txt |
false |
hochschulschrift_bool |
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doi_str |
10.1007/BF02841929 |
up_date |
2024-07-03T14:56:19.413Z |
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1803570201924468736 |
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