Please use this identifier to cite or link to this item:
|Title:||Progress towards the total synthesis of tedanolide: An efficient assembly of the C1-C11 subunit|
|Authors:||Loh, T.-P. |
|Citation:||Loh, T.-P., Feng, L.-C. (2001-08-20). Progress towards the total synthesis of tedanolide: An efficient assembly of the C1-C11 subunit. Tetrahedron Letters 42 (34) : 6001-6005. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(01)01169-8|
|Abstract:||The C1-C11 subunit of tedanolide was constructed using a boron-mediated syn aldol reaction as the key step to control the C6 and C7 stereocenters. Other features of this work include the asymmetric Sharpless dihydroxylation to incorporate the C2, C3 hydroxyl groups, selective protection of the hydroxyl group at C2 as well as the usage of a tert-butyl ester to tolerate the attack of Grignard and enolate reagents. © 2001 Elsevier Science Ltd. All rights reserved.|
|Source Title:||Tetrahedron Letters|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 10, 2018
WEB OF SCIENCETM
checked on Jun 27, 2018
checked on Jun 22, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.