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Results: 4
SYNTHESIS OF N-ALKOXYCARBONYL-3-SUBSTITUTED TETRAMIC ACIDS AND FUNCTIONALIZED ENOLS VIA C-ACYLATION REACTIONS OF ACTIVE METHYLENE-COMPOUNDSWITH N-HYDROXYSUCCINIMIDE ESTERS OF N-ALKOXYCARBONYL-ALPHA-AMINO ACIDS
Authors: DETSI A MICHASCRETTAS M IGGLESSIMARKOPOULOU O
Citation: A. Detsi et al., SYNTHESIS OF N-ALKOXYCARBONYL-3-SUBSTITUTED TETRAMIC ACIDS AND FUNCTIONALIZED ENOLS VIA C-ACYLATION REACTIONS OF ACTIVE METHYLENE-COMPOUNDSWITH N-HYDROXYSUCCINIMIDE ESTERS OF N-ALKOXYCARBONYL-ALPHA-AMINO ACIDS, Journal of the Chemical Society. Perkin transactions. I (Print), (15), 1998, pp. 2443-2449
THE TERT-BUTYL CHLORIDE-LITHIUM NAPHTHALENE RADICAL-ANION AND TERT-BUTYLLITHIUM-NAPHTHALENE SYSTEMS - MECHANISM OF METALATION (VOL 536, PG 149, 1997)
Authors: SCRETTAS CG MICHASCRETTAS M STEELE BR
Citation: Cg. Screttas et al., THE TERT-BUTYL CHLORIDE-LITHIUM NAPHTHALENE RADICAL-ANION AND TERT-BUTYLLITHIUM-NAPHTHALENE SYSTEMS - MECHANISM OF METALATION (VOL 536, PG 149, 1997), Journal of organometallic chemistry, 556(1-2), 1998, pp. 243-243
THE TERT-BUTYL CHLORIDE-LITHIUM NAPHTHALENE RADICAL-ANION AND TERT-BUTYLLITHIUM-NAPHTHALENE SYSTEMS - MECHANISM OF METALATION
Authors: SCRETTAS CG MICHASCRETTAS M STEELE BR
Citation: Cg. Screttas et al., THE TERT-BUTYL CHLORIDE-LITHIUM NAPHTHALENE RADICAL-ANION AND TERT-BUTYLLITHIUM-NAPHTHALENE SYSTEMS - MECHANISM OF METALATION, Journal of organometallic chemistry, 536(1-2), 1997, pp. 149-163
STOICHIOMETRY OF PROTONATION OF AROMATIC HYDROCARBON RADICAL-ANIONS BY WEAK PROTON DONORS - A MARKED DISCREPANCY BETWEEN THE NUMBER OF PROTONS USED AND THOSE INCORPORATED INTO THE AROMATIC STRUCTURE
Authors: SCRETTAS CG IOANNOU GI MICHASCRETTAS M
Citation: Cg. Screttas et al., STOICHIOMETRY OF PROTONATION OF AROMATIC HYDROCARBON RADICAL-ANIONS BY WEAK PROTON DONORS - A MARKED DISCREPANCY BETWEEN THE NUMBER OF PROTONS USED AND THOSE INCORPORATED INTO THE AROMATIC STRUCTURE, Journal of organometallic chemistry, 511(1-2), 1996, pp. 217-225
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