Complex Carbocycle by Photocycloaddition

Sieburth, Scott Mcneill

Abstract

Funding Agency

• Agency: National Institute of Health (NIH)
• Institute: National Institute of General Medical Sciences (NIGMS)
• Type: Research Project (R01)
• Project #: 5R01GM045214-06
• Application #: 2183007
• Study Section: Medicinal Chemistry Study Section (MCHA)
• Project Start: 1991-01-01
• Project End: 1998-06-30
• Budget Start: 1996-07-01
• Budget End: 1997-06-30
• Support Year: 6
• Fiscal Year: 1996

Institution

• Name: State University New York Stony Brook
• Department: Chemistry
• Type: Schools of Arts and Sciences
• DUNS #: 804878247
• City: Stony Brook
• State: NY
• Country: United States
• Zip Code: 11794

Publications

Lee, Y G; McGee Jr, K F; Chen, J et al. (2000) A [4 + 4] 2-pyridone approach to taxol. 3. Stereocontrol during elaboration of the cyclooctane. J Org Chem 65:6676-81

Sieburth, S M; McGee Jr, K F; Zhang, F et al. (2000) Photoreactivity of 2-pyridones with furan, benzene, and naphthalene. Inter- and intramolecular photocycloadditions. J Org Chem 65:1972-7

Sieburth, S M; McGee Jr, K F (1999) Solvent-dependent stereoselectivity of bis-2-pyridone [4 + 4] photocycloaddition is due to H-bonded dimers. Org Lett 1:1775-7