n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
The title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-propoxytetrahydro-2H-pyran-3,4,5-triyl triacetate], C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conf...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2013-02-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812051495 |
| _version_ | 1819288978553044992 |
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| author | Bettina Mönch Franziska Emmerling Werner Kraus Roland Becker Irene Nehls |
| author_facet | Bettina Mönch Franziska Emmerling Werner Kraus Roland Becker Irene Nehls |
| author_sort | Bettina Mönch |
| collection | DOAJ |
| description | The title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-propoxytetrahydro-2H-pyran-3,4,5-triyl triacetate], C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant interactions such as hydrogen bonds. |
| first_indexed | 2024-12-24T02:59:32Z |
| format | Article |
| id | doaj.art-40fb9611b13c45718e88129d6caeddd6 |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-24T02:59:32Z |
| publishDate | 2013-02-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-40fb9611b13c45718e88129d6caeddd62022-12-21T17:18:15ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682013-02-01692o158o15810.1107/S1600536812051495n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranosideBettina MönchFranziska EmmerlingWerner KrausRoland BeckerIrene NehlsThe title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-propoxytetrahydro-2H-pyran-3,4,5-triyl triacetate], C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant interactions such as hydrogen bonds.http://scripts.iucr.org/cgi-bin/paper?S1600536812051495 |
| spellingShingle | Bettina Mönch Franziska Emmerling Werner Kraus Roland Becker Irene Nehls n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside Acta Crystallographica Section E |
| title | n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside |
| title_full | n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside |
| title_fullStr | n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside |
| title_full_unstemmed | n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside |
| title_short | n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside |
| title_sort | n propyl 2 3 4 6 tetra o acetyl 946 d glucopyranoside |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536812051495 |
| work_keys_str_mv | AT bettinam246nch npropyl2346tetraoacetyl946dglucopyranoside AT franziskaemmerling npropyl2346tetraoacetyl946dglucopyranoside AT wernerkraus npropyl2346tetraoacetyl946dglucopyranoside AT rolandbecker npropyl2346tetraoacetyl946dglucopyranoside AT irenenehls npropyl2346tetraoacetyl946dglucopyranoside |