This proposal focuses on the application of pericyclic reactions in new methodology for the synthesis of several important classes of carbocyclic and heterocyclic organic compounds. Part I describes the development of new strategies for the synthesis of five- and sixmembered aromatic, heteroaromatic, and dihydroaromatic systems. Intramolecular (4+2) cycloaddition reactions of conjugated enynes will be investigated and employed in new routes to highly condensed polycyclic systems. Heterocyclic variants of this process will be developed leading to five- and six-membered nitrogen and oxygen heterocycles. The application of this chemistry to the synthesis of furanophenalenone diterpenes, pentacyclic polyketide marine natural products with protein tyrosine kinase inhibitory activity, and to the synthesis of the antiviral agent nothapodytine B (mappicine ketone) will also be examined. Part II of the proposal describes the development of new methods for the synthesis of conjugated, unsaturated ketenes and their use in new annulation strategies for the synthesis of five-, six-, and seven-membered carbocyclic and heterocyclic compounds. Part III of the proposal describes the application of a tandem propargylic rearrangement-asymmetric inverse electron-demand intramolecular vinylallene Diels-Alder strategy in an exceptionally concise approach to the total synthesis of the nematode hatching stimulus agent glycinoeclepin A.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM028273-24
Application #
6726770
Study Section
Medicinal Chemistry Study Section (MCHA)
Program Officer
Schwab, John M
Project Start
1980-07-01
Project End
2006-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
24
Fiscal Year
2004
Total Cost
$290,846
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Willumstad, Thomas P; Boudreau, Paul D; Danheiser, Rick L (2015) Synthesis of Highly Substituted Quinolines via a Tandem Ynamide Benzannulation/Iodocyclization Strategy. J Org Chem 80:11794-805
Lam, Tin Yiu; Wang, Yu-Pu; Danheiser, Rick L (2013) Benzannulation via the reaction of ynamides and vinylketenes. application to the synthesis of highly substituted indoles. J Org Chem 78:9396-414
Willumstad, Thomas P; Haze, Olesya; Mak, Xiao Yin et al. (2013) Batch and flow photochemical benzannulations based on the reaction of ynamides and diazo ketones. Application to the synthesis of polycyclic aromatic and heteroaromatic compounds. J Org Chem 78:11450-69
Lan, Yu; Danheiser, Rick L; Houk, K N (2012) Why nature eschews the concerted [2 + 2 + 2] cycloaddition of a nonconjugated cyanodiyne. Computational study of a pyridine synthesis involving an ene-Diels-Alder-bimolecular hydrogen-transfer mechanism. J Org Chem 77:1533-8
Wang, Yu-Pu; Danheiser, Rick L (2011) Synthesis of 2-iodoynamides and regioselective [2+2] cycloadditions with ketene. Tetrahedron Lett 52:2111-2114
Benda, Konstantin; Knoth, Tanja; Danheiser, Rick L et al. (2011) A New Route to Silyl-substituted Cyclobutenones and Silylketenes. Tetrahedron Lett 52:46-48
Robinson, Julia M; Tlais, Sami F; Fong, Jennie et al. (2011) A [4 + 4] annulation strategy for the synthesis of eight-membered carbocycles based on intramolecular cycloadditions of conjugated enynes. Tetrahedron 67:9890-9898
Mak, Xiao Yin; Crombie, Aimee L; Danheiser, Rick L (2011) Synthesis of polycyclic benzofused nitrogen heterocycles via a tandem ynamide benzannulation/ring-closing metathesis strategy. Application in a formal total synthesis of (+)-FR900482. J Org Chem 76:1852-73
Robinson, Julia M; Sakai, Takeo; Okano, Katsuhiko et al. (2010) Formal [2 + 2 + 2] cycloaddition strategy based on an intramolecular propargylic ene reaction/Diels-Alder cycloaddition cascade. J Am Chem Soc 132:11039-41
Sakai, Takeo; Danheiser, Rick L (2010) Cyano Diels-Alder and cyano ene reactions. Applications in a formal [2 + 2 + 2] cycloaddition strategy for the synthesis of pyridines. J Am Chem Soc 132:13203-5

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