The use of target-directed synthesis as inspiration for the discovery of novel reactions gives access to new, medicinally relevant structures and general methods for their synthesis, as well as new synthetic methodologies that will benefit an array of diverse applications. Ultimately, any development that enhances our ability to assemble compounds more efficiently will have a profound impact upon biology and human medicine through medicinal chemistry and process research and development. This application describes the development of a novel reaction methodology for the enantioselective formation of vicinal quaternary and tertiary stereocenters. Specifically, the research strategy exploits this methodology to outline a synthetic route to the natural product isopalhinine A. Isopalhinine A is a Lycopodium alkaloid with the most sterically congested and structurally complex framework of all the members of the family. Since its isolation in 2013, no completed synthesis has been reported to date. In this multifaceted and integrated program, we hypothesize that expanding the scope of our laboratory's recently developed iridium-catalyzed allylic alkylation chemistry from aryl- and alkenyl-substituted allyl carbonates to include alkyl-substituted electrophiles will facilitate a concise, enantioselective synthesis of isopalhinine A.
The specific aims of this application are: 1) the expansion of iridium-catalyzed asymmetric allylic alkylation chemistry with prochiral carbon nucleophiles to include alkyl-substituted electrophiles, 2) total synthesis of isopalhinine A: construction of the spirocyclic intermediate, and 3) total synthesis of isopalhinine A: intramolecular Diels-Alder reaction and final modifications. The described expansion in the field of iridium-catalyzed allylic alkylation chemistry as well as the additional innovation embedded within the strategies and tactics employed in the total synthesis will ultimately lead to the more efficient assembly of other complex bioactive targets and, broadly, the discovery of new therapeutics.

Public Health Relevance

Organic synthesis is fueled by the development of new methods for converting simple molecular building blocks into complex structures with precise control over atom connectivity. Ultimately, any development in organic synthesis that enhances our ability to assemble compounds more efficiently will have a profound impact upon biology and human medicine through improved drug discovery and manufacture. This proposal outlines a new approach toward constructing important molecular linkages and the implementation of this method in a highly complex synthetic target of relevance to human medicine.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31GM120804-02
Application #
9336167
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Barski, Oleg
Project Start
2016-07-01
Project End
2018-06-30
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
009584210
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Hethcox, J Caleb; Shockley, Samantha E; Stoltz, Brian M (2018) Enantioselective Synthesis of Vicinal All-Carbon Quaternary Centers via Iridium-Catalyzed Allylic Alkylation. Angew Chem Int Ed Engl 57:8664-8667
Hethcox, J Caleb; Shockley, Samantha E; Stoltz, Brian M (2017) Enantioselective Iridium-Catalyzed Allylic Alkylation Reactions of Masked Acyl Cyanide Equivalents. Org Lett 19:1527-1529
Shockley, Samantha E; Hethcox, J Caleb; Stoltz, Brian M (2017) Enantioselective Synthesis of Acyclic ?-Quaternary Carboxylic Acid Derivatives through Iridium-Catalyzed Allylic Alkylation. Angew Chem Int Ed Engl 56:11545-11548
Hethcox, J Caleb; Shockley, Samantha E; Stoltz, Brian M (2016) Iridium-Catalyzed Stereoselective Allylic Alkylation Reactions with Crotyl Chloride. Angew Chem Int Ed Engl 55:16092-16095
Hethcox, J Caleb; Shockley, Samantha E; Stoltz, Brian M (2016) Iridium-Catalyzed Diastereo-, Enantio-, and Regioselective Allylic Alkylation with Prochiral Enolates. ACS Catal 6:6207-6213