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Results: 6

Authors: BURES E SPINAZZE PG BEESE G HUNT IR ROGERS C KEAY BA
Citation: E. Bures et al., REGIOSELECTIVE PREPARATION OF 2,4-SUBSTITUTED, 3,4-SUBSTITUTED, AND 2,3,4-SUBSTITUTED FURAN RINGS .1. [1,4]O-]C AND [1,4]C-]O SILYL MIGRATIONS OF SILYL ETHERS AND ESTERS ATTACHED TO FURAN AND THIOPHENE RINGS, Journal of organic chemistry, 62(25), 1997, pp. 8741-8749

Authors: BURES E NIEMAN JA YU SY SPINAZZE PG BONTRONT JLJ HUNT IR RAUK A KEAY BA
Citation: E. Bures et al., REGIOSELECTIVE PREPARATION OF 2,4-SUBSTITUTED, 3,4-SUBSTITUTED, AND 2,3,4-SUBSTITUTED FURAN RINGS .2. REGIOSELECTIVE LITHIATION OF 2-SILYLATED-3-SUBSTITUTED FURAN RINGS, Journal of organic chemistry, 62(25), 1997, pp. 8750-8759

Authors: CARPENTER BE HUNT IR KEAY BA
Citation: Be. Carpenter et al., A SHORT EFFICIENT PREPARATION OF (-TRANS-2-PHENYLCYCLOHEXANOL AND (-)-TRANS-2-PHENYLCYCLOHEXANOL()), Tetrahedron : asymmetry, 7(11), 1996, pp. 3107-3108

Authors: HUNT IR RAUK A KEAY BA
Citation: Ir. Hunt et al., WHY DO CATALYTIC QUANTITIES OF LEWIS-ACID GENERALLY YIELD MORE PRODUCT THAN 1.1 EQUIV IN THE INTRAMOLECULAR DIELS-ALDER REACTION WITH A FURAN DIENE .2. AM1 CALCULATIONS AND MATHEMATICAL SIMULATION OF THE EQUILIBRIA, Journal of organic chemistry, 61(2), 1996, pp. 751-757

Authors: HUNT IR ROGERS C WOO S RAUK A KEAY BA
Citation: Ir. Hunt et al., WHY DO CATALYTIC QUANTITIES OF LEWIS-ACID GENERALLY YIELD MORE PRODUCT THAN 1.1-EQUIV IN THE INTRAMOLECULAR DIELS-ALDER REACTION WITH A FURAN DIENE - COMPETITIVE COMPLEXATION NMR-STUDIES PROVIDE AN ANSWER, Journal of the American Chemical Society, 117(3), 1995, pp. 1049-1056

Authors: RAUK A HUNT IR KEAY BA
Citation: A. Rauk et al., LEWIS ACIDITY AND BASICITY - AN AB-INITIO STUDY OF PROTON AND BF3 AFFINITIES OF OXYGEN-CONTAINING ORGANIC-COMPOUNDS, Journal of organic chemistry, 59(22), 1994, pp. 6808-6816
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