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Zinc-proline catalyzed pathway for the formation of sugars
Zn-proline catalyzes the aldolisation of unprotected glycolaldehyde in water to give tetroses and hexoses; threose (33% of the product mixture) was formed with 10% enantiomeric excess of the D-isomer.
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| Published in: | Chemical communications (Cambridge, England) England), 2004-07 (13), p.1540-1541 |
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| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c345t-39e2aa53c48e45031864fbbce4e431415421c3919c13fe20451ad84cbd2e60393 |
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| cites | cdi_FETCH-LOGICAL-c345t-39e2aa53c48e45031864fbbce4e431415421c3919c13fe20451ad84cbd2e60393 |
| container_end_page | 1541 |
| container_issue | 13 |
| container_start_page | 1540 |
| container_title | Chemical communications (Cambridge, England) |
| container_volume | |
| creator | Kofoed, Jacob Machuqueiro, Miguel Reymond, Jean-Louis Darbre, Tamis |
| description | Zn-proline catalyzes the aldolisation of unprotected glycolaldehyde in water to give tetroses and hexoses; threose (33% of the product mixture) was formed with 10% enantiomeric excess of the D-isomer. |
| doi_str_mv | 10.1039/b404465g |
| format | article |
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| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2004-07 (13), p.1540-1541 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_66644792 |
| source | Royal Society of Chemistry: Jisc Collections: Journals Archive 1841-2007 (2019-2023) |
| subjects | Acetaldehyde - analogs & derivatives Acetaldehyde - chemistry Carbohydrates - chemical synthesis Catalysis Hexoses - chemical synthesis Molecular Structure Proline - chemistry Solutions Stereoisomerism Tetroses - chemical synthesis Zinc - chemistry |
| title | Zinc-proline catalyzed pathway for the formation of sugars |
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