Synthesis of Resorcinols via a Michael Addition-Dieckman Cyclization Sequence of Dimethyl 1,3-Acetonedicarboxylate Anion with Alkyl Alkynoates
摘要:
The reaction of dimethyl 1,3-acetonedicarboxylate anion 1 with a number of alkyl alkynoates gives unsymmetrical (from alkynoates 2a-g) or symmetrical (from alkynoates 2h-i) resorcinols, in a one pot synthesis.
Synthesis of functionally substituted furan and resorcinol derivatives from dimethyl 3-oxopentanedioate
作者:V. M. Ismailov、G. G. Ibragimova、N. D. Sadykhova、Z. A. Mamedova、N. N. Yusubov
DOI:10.1134/s1070428017060239
日期:2017.6
The alkylation of dimethyl 3-oxopentanedioate with 1,2-dibromoethane and 1,2,3-tribromopropane afforded C,C-(cyclopropane derivative) and C,O-dialkylation products. The initial trioxo compound underwent partial self-condensation to produce resorcinolderivative.
Crombie, Leslie; Games, David E.; James, Alun W. G., Journal of the Chemical Society. Perkin transactions I, 1996, # 22, p. 2715 - 2724
作者:Crombie, Leslie、Games, David E.、James, Alun W. G.
DOI:——
日期:——
Synthesis of Resorcinols via a Michael Addition-Dieckman Cyclization Sequence of Dimethyl 1,3-Acetonedicarboxylate Anion with Alkyl Alkynoates
作者:A. Covarrubias-Zúñiga、L. A. Maldonado、E. Ríos-Barrios、A. González-Lucas
DOI:10.1080/00397919808004454
日期:1998.9
The reaction of dimethyl 1,3-acetonedicarboxylate anion 1 with a number of alkyl alkynoates gives unsymmetrical (from alkynoates 2a-g) or symmetrical (from alkynoates 2h-i) resorcinols, in a one pot synthesis.
Koller; Krakauer, Monatshefte fur Chemie, 1929, vol. 53/54, p. 946