WebNov 7, 2024 · In the case of bishomoallylic alcohols, an intriguing ligand-induced divergent reactivity was observed. A terminal-to-internal alkene isomerization promoted by Rh/L7 followed by redox isomerization using Rh/BINAP system produced chiral ketones bearing a γ-stereocenter with high yield and enantioselectivity. Mechanistic studies … WebMar 20, 2024 · The quinoxalinonyl-functionalization of alkenes employs the quinoxalinone-substituted tertiary bishomoallylic alcohols as substrates, proceeds through …
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Web3 Bishomoallylic Alcohols 1-Phenylpent-4-en-1-ol (1a),1,2 1-phenylhex-4-en-1-ol (1b),1 2-phenylpent-4-en-1-ol (1d),3 3-phenylpent-4-en-1-ol (1e),1,4 trans- and cis-2-allylcyclohexanol (1f–g)5 and 2-methyl-1,3-bis(2,4,5-trimethoxyphenyl)pent-4-en-1-ol (1h)6 were prepared according to published procedures. (E)-Methyl 6-hydroxy-6-phenylhex-2 ... WebJan 23, 2024 · This review describes three fascinating and attractive topics in enantioselective substrate-directed epoxidation: (1) carboxylic acid- or amine derivative-directed epoxidation, (2) regioselective epoxidation of non-proximal alkenes, (3) enantioselective epoxidation of bishomoallylic alcohols. Supporting Information … east greenwich to springfield ma
Modular Design of Chiral Conjugate-Base-Stabilized Carboxylic …
WebSep 9, 2024 · Readily available 1,2-amino alcohols provide the framework for a new generation of chiral carboxylic acid catalysts that rival the acidity of the widely used chiral phosphoric acid catalyst (S)-TRIP. Covalently linked thiourea sites stabilize the carboxylate conjugate bases of these catalysts … WebA palladium-catalyzed hydroalkylation reaction of protected allylic alcohols using alkylzinc bromide reagents is reported. This account includes numerous allylic, homoallylic, and bishomoallylic alcohol derivatives, all with a uniform selectivity of >20:1 for the anti-Markovnikov product. WebSeveral standout advances have been reported. In the field of oxidation, Yamamoto has reported methods for the reliable enantioselective epoxidation of homoallylic and bishomoallylic alcohols (H. Yamamoto, J. Am. Chem. Soc., 2010, ) an area hitherto underdeveloped in comparison with allylic alcohol oxidation. culligan water systems panama city fl