ICAR Research Data Repository for Knowledge Management
Total Syntheses of All Stereoisomers of Phenatic Acid B
DSpace at IIT Bombay
View Archive Info| Field | Value | |
| Title |
Total Syntheses of All Stereoisomers of Phenatic Acid B
|
|
| Creator |
FERNANDES, RA
CHOWDHURY, AK |
|
| Subject |
asymmetric dihydroxylation
claisen rearrangement polyvalent iodine chemistry |
|
| Description |
The total syntheses of all stereoisomers of phenatic acid B and determination of their absolute configuration are described. The synthetic strategy is based on all efficient combination of the Sharpless asymmetric dihydroxylation, the Johnson-Claisen rearrangement, and hydroboration-oxidation. It involves 11-12 steps and overall yield of 5-8%.
|
|
| Publisher |
AMER CHEMICAL SOC
|
|
| Date |
2011-07-15T03:06:23Z
2011-12-26T12:49:12Z 2011-12-27T05:35:00Z 2011-07-15T03:06:23Z 2011-12-26T12:49:12Z 2011-12-27T05:35:00Z 2009 |
|
| Type |
Article
|
|
| Identifier |
JOURNAL OF ORGANIC CHEMISTRY, 74(22), 8826-8829
0022-3263 http://dx.doi.org/10.1021/jo901927w http://dspace.library.iitb.ac.in/xmlui/handle/10054/4139 http://hdl.handle.net/10054/4139 |
|
| Language |
en
|
|