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Pure Appl. Chem., 1997, Vol. 69, No. 3, pp. 609-614

http://dx.doi.org/10.1351/pac199769030609

Natural products synthesis involving anions derived from functionalized mono- and diesters

Y. Thebtaranonth

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  • Phutdhawong Weerachai, Eksinitkun Gedsirin, Pyne Stephen G., Willis Anthony C., Phutdhawong Waya S.: Stereoselective synthesis of α-methylenecyclopentenones via a Diels–Alder/retro-Diels–Alder protocol. Tetrahedron 2013, 69, 9270. <http://dx.doi.org/10.1016/j.tet.2013.08.046>
  • Choommongkol Ruangrat, Jongkol Rattana, Prabpai Samran, Kongsaeree Palangpon, Meepowpan Puttinan: Synthesis of racemic and optically active forms of novel antimalarial agents, spirocyclopentanone–anthracene adducts, via tandem Michael addition–Dieckmann condensation reactions as the key steps. Tetrahedron: Asymmetry 2012, 23, 357. <http://dx.doi.org/10.1016/j.tetasy.2012.03.006>
  • Basabe P., Blanco A., Marcos I.S., Díez D., Bodero O., Martín M., Urones J.G.: Synthesis of spongidines A and D: marine metabolites phospholipase A2 inhibitors. Tetrahedron 2011, 67, 3649. <http://dx.doi.org/10.1016/j.tet.2011.03.084>
  • Demuynck Anneleen L. W., Levecque Pieter, Kidane Aklilu, Gammon David W., Sickle Eugene, Jacobs Pierre A., De Vos Dirk E., Sels Bert F.: Retro-Diels-Alder Reactions of Masked Cyclopentadienones Catalyzed by Heterogeneous Brønsted Acids. Adv Synth Catal 2010, 352, 3419. <http://dx.doi.org/10.1002/adsc.201000571>
  • Jongkol Rattana, Choommongkol Ruangrat, Tarnchompoo Bongkoch, Nimmanpipug Piyarat, Meepowpan Puttinan: Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction–lactonization. Tetrahedron 2009, 65, 6382. <http://dx.doi.org/10.1016/j.tet.2009.06.016>
  • Thirumamagal B.T.S., Narayanasamy Sureshbabu: Formation of 2-arylindane-1,3-diones and 3-alkylphthalides from methyl o-[α-phenylsulfonyl]toluate. Tetrahetron Lett 2008, 49, 512. <http://dx.doi.org/10.1016/j.tetlet.2007.11.091>
  • Kongsaeree Palangpon, Meepowpan Puttinan, Thebtaranonth Yodhathai: Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol–lactonization reactions. Tet Asymm 2001, 12, 1913. <http://dx.doi.org/10.1016/S0957-4166(01)00345-7>
  • Lertvorachon Jittiwud, Meepowpan Puttinan, Thebtaranonth Yodhathai: An aldol - bislactonization route to α-methylene bis-γ-butyrolactones. Tetrahedron 1998, 54, 14341. <http://dx.doi.org/10.1016/S0040-4020(98)00888-6>