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Citation: A. Glekas et Sm. Sieburth, Studies in silanol synthesis: internal nucleophiles and steric hindrance, TETRAHEDR L, 42(23), 2001, pp. 3799-3801
Citation: Kf. Mcgee et al., Fusicoccin synthesis by intramolecular [4+4] photocycloaddition of 2-pyridones: Stereocontrol of the cycloaddition and elaboration of the pentacyclicproduct, SYNTHESIS-S, (8), 2001, pp. 1185-1196
Citation: Yp. Chen et al., Pyridone annulation by 4+2 coupling of dienolates with nitriles and nitrile equivalents. A solution to the acetonitrile problem, J ORG CHEM, 66(20), 2001, pp. 6826-6828
Citation: Gw. Hewitt et al., Synthesis of alpha-alkyl-alpha-aminosilanes by rhodium-catalyzed hydrosilylation of Boc-protected vinyl amines, TETRAHEDR L, 41(52), 2000, pp. 10175-10179
Authors:
Sieburth, SM
McGee, KF
Zhang, FN
Chen, YP
Citation: Sm. Sieburth et al., Photoreactivity of 2-pyridones with furan, benzene, and naphthalene. Inter- and intramolecular photocycloadditions, J ORG CHEM, 65(7), 2000, pp. 1972-1977
Authors:
Lee, YG
McGee, KF
Chen, JH
Rucando, D
Sieburth, SM
Citation: Yg. Lee et al., A [4+4] 2-pyridone approach to taxol. 3. Stereocontrol during elaboration of the cyclooctane, J ORG CHEM, 65(20), 2000, pp. 6676-6681
Citation: Sm. Sieburth et Kf. Mcgee, Solvent-dependent stereoselectivity of bis-5-pyridone [4+4] photocycloaddition is due to H-bonded dimers, ORG LETT, 1(11), 1999, pp. 1775-1777
Citation: T. Nittoli et al., Evidence for helicity in insect diuretic peptide hormones: computational analysis, spectroscopic studies, and biological assays, J PEPT RES, 53(2), 1999, pp. 99-108
Citation: Sm. Sieburth, The inter- and intramolecular [4+4] photocycloaddition of 2-pyridones and its application to natural product synthesis, ADV CYCLOAD, 5, 1999, pp. 85-118
Citation: Sm. Sieburth et J. Lang, A practical synthesis of difunctional organosilane reagents and their application to the Diels-Alder reaction, J ORG CHEM, 64(6), 1999, pp. 1780-1781
Citation: Sm. Sieburth et al., Selective intermolecular photo-[4+4]-cycloaddition with 8-pyridone mixtures. 3. Synthetic transformations of the trans cross-product (1 alpha,2 beta,5 beta,6 alpha)-3-butyl-9-methoxy-3,7-diazatricyclo[4.2.2.2(2,5)]dodeca-9,11-diene-4,8-dione, J ORG CHEM, 64(3), 1999, pp. 954-959