Total synthesis of parvaquone and the serendipitous discovery of a novel chromium-mediated method for β-lactone formation
摘要:
During attempts to synthesise the 2-hydroxy-1,4-naphthoquinone, parvaquone, 1, a novel chromium-mediated method for the synthesis of functionalised p-lactones from propargyl alcohols has been discovered. Additionally, using both dry state and ultrasound conditions, the total synthesis of parvaquone (I) has been achieved; the most efficient techniques deliver this target compound in up to 46% overall yield over, as low as, two synthetic processes.
Braams,J.F.H. et al., Recueil des Travaux Chimiques des Pays-Bas, 1972, vol. 91, p. 700 - 710
作者:Braams,J.F.H. et al.
DOI:——
日期:——
Lukashev, N. V.; Artyushin, O. I.; Poznyatovskii, V. A., Journal of general chemistry of the USSR, 1984, vol. 54, # 10, p. 2136 - 2137
作者:Lukashev, N. V.、Artyushin, O. I.、Poznyatovskii, V. A.、Grishin, Yu. K.、Kazankova, M. A.、Lutsenko, I. F.
DOI:——
日期:——
Tane, Jeffrey P.; Vollhardt, K. Peter C., Angewandte Chemie, 1982, vol. 94, p. 642 - 643
作者:Tane, Jeffrey P.、Vollhardt, K. Peter C.
DOI:——
日期:——
Novel bicyclic oxazolone derivatives as anti-Angiogenic agents
作者:Françoise M Perron-Sierra、Alain Pierré、Mike Burbridge、Nicolas Guilbaud
DOI:10.1016/s0960-894x(02)00197-x
日期:2002.6
Novel bicyclic tetrahydropyrano[3,2-4]oxazolones derivatives, analogues of Fumagillin, were synthesised via a stereo-controlled oxidative-rearrangement of furylcarbinols and subsequent treatment with the appropriate isocyanate. These compounds demonstrated potent antiangiogenic activity. (C) 2002 Elsevier Science Ltd. All rights reserved.
LUKASHEV, N. V.;ARTYUSHIN, O. I.;ROZNYATOVSKIJ, V. A.;GRISHIN, YU. K.;KAZ+, ZH. OBSHCH. XIMII, 1984, 54, N 10, 2390-2391
作者:LUKASHEV, N. V.、ARTYUSHIN, O. I.、ROZNYATOVSKIJ, V. A.、GRISHIN, YU. K.、KAZ+