Journal of the Chemical Society. Chemical communications p. 760 - 761 (1988)
Update date:2022-08-05
Topics: Regioselectivity Diastereoselectivity Column chromatography Yield NMR spectroscopy Catalyst Nucleophile Electrophile Enantiomeric excess (ee) Deprotonation Mass spectrometry (MS) Cyclization Stereoselective Retrosynthetic analysis Substrate Chiral Auxiliary Reaction Optimization Ring Strain
Kim, Deukjoon
Jang, Yoo Mi
Kim, In O
Park, Sang Woo
Intramolecular alkylation of the enolates derived from the esters (3) and (7) stereoselectively afforded the cyclopentanecarboxylate (4) and the cyclobutanecarboxylate (8), respectively; compound (8) is a potential intermediate for the synthesis of (+/-)-
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Doi:10.1039/c8sc01016a
(2018)Doi:10.1016/S0040-4020(01)90079-1
(1990)Doi:10.1055/s-1990-27090
(1990)Doi:10.1007/BF00766551
(1990)Doi:10.1039/P19910000215
(1991)Doi:10.1016/0039-128X(91)90072-4
(1991)
