Published October 28, 2014
| Supplemental Material + Published
Journal Article
Open
Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation
Chicago
Abstract
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables the formal total syntheses of a number of "classic" natural product target molecules. This publication highlights recent methods for setting quaternary and tetrasubstituted tertiary carbon stereocenters to address the synthetic hurdles encountered over many decades across multiple compound classes spanning carbohydrate derivatives, terpenes, and alkaloids. These enantioselective methods will impact both academic and industrial settings, where the synthesis of stereogenic quaternary carbons is a continuing challenge.
Additional Information
© 2014, Liu et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc). Received: 11 August 2014. Accepted: 09 October 2014. Published: 28 October 2014. Associate Editor: S. Bräse. We are grateful to NIH (R01GM080269), Amgen, the Gordon and Betty Moore Foundation, and Caltech for funding. We also thank the Caltech Minorities Undergraduate Research Fellowship program, PREM program, Eli Lilly, the Resnick Sustainability Institute at Caltech (fellowship for Y. L.), and the Swiss National Science Foundation (SNSF, fellowship for M. L.). Dr. Michael L. Krout and Dr. David E. White are acknowledged for preliminary experimental work related to their results. Dr. Michael Takase (Caltech) and Larry Henling (Caltech) are gratefully acknowledged for X-ray crystallographic structural determination.Attached Files
Published - 1860-5397-10-261.pdf
Supplemental Material - Beilstein_J_Org_Chem-10-2501-s001.pdf
Files
1860-5397-10-261.pdf
Files
(3.6 MB)
Name | Size | Download all |
---|---|---|
md5:13d0b84192b0401e1dce4c0eecd4a309
|
879.3 kB | Preview Download |
md5:70c22b742e93d3428c38d5a01168ecd8
|
2.7 MB | Preview Download |
Additional details
- PMCID
- PMC4222294
- Eprint ID
- 52797
- Resolver ID
- CaltechAUTHORS:20141215-084337170
- NIH
- R01GM080269
- Amgen
- Gordon and Betty Moore Foundation
- Caltech
- Caltech Minorities Undergraduate Research Fellowship (MURF)
- PREM program
- Eli Lilly
- Resnick Sustainability Institute
- Swiss National Science Foundation (SNSF)
- Created
-
2014-12-15Created from EPrint's datestamp field
- Updated
-
2021-11-10Created from EPrint's last_modified field
- Caltech groups
- Resnick Sustainability Institute