A study is proposed of the Lewis Acid and/or pressure promoted Diels-Alder reactions of 3-methyl-2H-thiopyran, I, its 4- and/or 6-trialkylsilyloxy derivatives and their 2H-pyran analogs with 2,6-dimethyl-p-quinone and 2-methoxy-6-methyl-p-quinone, II. The expected major adduct under these conditions is III. The reaction of I and II to give III will provide an entry into a novel and general strategy for the synthesis of the nagilactones, inumakilactones, hallactones and podolactones, members of a large group of diterpene dilactones possessing the basic structure IV. These naturally occurring compounds display important antitumor, antibiotic and insecticidal properties and contrasting plant growth regulatory activity. The most biologically active members, nagilactone F and antibiotic LL-Z1271Alpha, are targeted for total synthesis to demonstrate the validity of the strategy. An additional objective of this research is to investigate the effects of very high pressure (15Kbar) on potential cis-dienethione/cis-dienone reversible 2H-thiopyran/2H-pyran equilibria.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM037003-02
Application #
3291806
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1986-08-01
Project End
1989-07-31
Budget Start
1987-08-01
Budget End
1988-07-31
Support Year
2
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Kansas Lawrence
Department
Type
Schools of Arts and Sciences
DUNS #
072933393
City
Lawrence
State
KS
Country
United States
Zip Code
66045