Published June 19, 2015
| Supplemental Material
Journal Article
Open
Exceedingly Efficient Synthesis of (±)-Grandifloracin and Acylated Analogues
Chicago
An error occurred while generating the citation.
Abstract
A highly efficient regio- and stereoselective total synthesis of (±)-grandifloracin via a tandem dearomative epoxidation/spontaneous Diels–Alder cyclodimerization from salicylic acid in only four steps is reported. The synthetic route allows for late-stage diversification of the core structure to give ready access to analogues of this promising agent against pancreatic cancer.
Additional Information
© 2015 American Chemical Society. Received: May 1, 2015. Publication Date (Web): June 10, 2015. The authors wish to thank NSF (1265591), Amgen, and Caltech for financial support. M.B. thanks the Drug Research Academy and the Danish Cancer Society for financial support. D.C.D. (Caltech) thanks the National Science Foundation for financial support (Predoctoral Research Fellowship, No. DGE-1144469). L.C. (Caltech) is grateful to the Arthur R. Adams SURF Endowment. The Caltech Center for Catalysis and Chemical Synthesis (C3S) and especially Dr. Scott Virgil (Caltech) are acknowledged for help with chiral separation. Dr. Michael K. Takase (Caltech) is acknowledged for X-ray crystallographic structural determination.Attached Files
Supplemental Material - ol5b01292_si_001.pdf
Files
ol5b01292_si_001.pdf
Files
(725.3 kB)
| Name | Size | Download all |
|---|---|---|
|
md5:faadd2118eaaa3527d8caeb6dda1b316
|
725.3 kB | Preview Download |
Additional details
- Eprint ID
- 58230
- Resolver ID
- CaltechAUTHORS:20150615-081527494
- NSF
- 1265591
- Amgen
- Caltech
- Drug Research Academy
- Danish Cancer Society
- NSF Graduate Research Fellowship
- DGE-1144469
- Arthur R. Adams SURF Endowment
- Caltech Summer Undergraduate Research Fellowship (SURF)
- Created
-
2015-06-15Created from EPrint's datestamp field
- Updated
-
2021-11-10Created from EPrint's last_modified field