Abstract
A regio- and stereoselective intramolecular direct aldol reaction of 2,7-diketones derived from carbohydrates has been developed to construct cycloalkanones 7, which were dehydrated to obtain heavily oxygenated cycloalkenones 8.
| Original language | English |
|---|---|
| Pages (from-to) | 4795-4802 |
| Number of pages | 8 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 13 |
| Issue number | 16 |
| DOIs | |
| Publication status | Published - 2015 Apr 28 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
Cite this
Intramolecular direct aldol reactions of sugar 2,7-diketones : Syntheses of hydroxylated cycloalka(e)nones. / Shing, Tony Kung Ming; Cheng, Hau M.
In: Organic and Biomolecular Chemistry, Vol. 13, No. 16, 28.04.2015, p. 4795-4802.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Intramolecular direct aldol reactions of sugar 2,7-diketones
T2 - Syntheses of hydroxylated cycloalka(e)nones
AU - Shing, Tony Kung Ming
AU - Cheng, Hau M.
PY - 2015/4/28
Y1 - 2015/4/28
N2 - A regio- and stereoselective intramolecular direct aldol reaction of 2,7-diketones derived from carbohydrates has been developed to construct cycloalkanones 7, which were dehydrated to obtain heavily oxygenated cycloalkenones 8.
AB - A regio- and stereoselective intramolecular direct aldol reaction of 2,7-diketones derived from carbohydrates has been developed to construct cycloalkanones 7, which were dehydrated to obtain heavily oxygenated cycloalkenones 8.
UR - http://www.scopus.com/inward/record.url?scp=84927584277&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84927584277&partnerID=8YFLogxK
U2 - 10.1039/c5ob00253b
DO - 10.1039/c5ob00253b
M3 - Article
AN - SCOPUS:84927584277
VL - 13
SP - 4795
EP - 4802
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 16
ER -