Journal article
Triacetonide of Glucoheptonic Acid in the Scalable Syntheses of d-Gulose, 6-Deoxy-d-gulose, l-Glucose, 6-Deoxy-l-glucose, and Related Sugars.
- Abstract:
- Ease of separation of petrol-soluble acetonides derived from the triacetonide of methyl glucoheptonate allows scalable syntheses of rare sugars containing the l-gluco or d-gulo structural motif with any oxidation level at the C6 or C1 position of the hexose, usually without chromatography: meso-d-glycero-d-guloheptitol available in two steps is an ideal entry point for the study of the biotechnological production of heptoses.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Accepted manuscript, pdf, 633.7KB, Terms of use)
-
- Publisher copy:
- 10.1021/acs.orglett.6b02041
Authors
Funding
Bibliographic Details
- Publisher:
- American Chemical Society
- Journal:
- Organic Letters More from this journal
- Volume:
- 18
- Issue:
- 16
- Pages:
- 4112-4115
- Publication date:
- 2016-08-03
- Acceptance date:
- 2016-08-02
- DOI:
- EISSN:
-
1523-7052
- ISSN:
-
1523-7060
- Pmid:
-
27487167
Item Description
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:638246
- UUID:
-
uuid:f0e8ef12-a8cc-482d-abd3-1ecc24a4bed2
- Local pid:
-
pubs:638246
- Source identifiers:
-
638246
- Deposit date:
-
2016-09-09
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2016
- Notes:
- © 2016 American Chemical Society. This is the accepted manuscript version of the article. The final version is available online from ACS at: [10.1021/acs.orglett.6b02041]
Metrics
If you are the owner of this record, you can report an update to it here: Report update to this record