CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 1987, Vol. 59, No. 3, pp. 345-352

http://dx.doi.org/10.1351/pac198759030345

Iterative butenolide construction of polypropionate chains. Application to an efficient synthesis of (+)(9S)-dihydroerythronolide A

G. Stork and S. D. Rychnovsky

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Gao Xin, Woo Sang Kook, Krische Michael J.: Total Synthesis of 6-Deoxyerythronolide B via C–C Bond-Forming Transfer Hydrogenation. J. Am. Chem. Soc. 2013, 135, 4223. <http://dx.doi.org/10.1021/ja4008722>
  • Woo King-Chung, Jones Keith: Asymmetric synthesis from α-amino acids; some reactions of (S)-pyroglutamate. Tetrahetron Lett 1991, 32, 6949. <http://dx.doi.org/10.1016/0040-4039(91)80452-C>
  • Shimizu Isao, Maruyama Takashi, Hasegawa Hajime: Facile Synthesis of .ALPHA.-Hydroxybutenolides and .ALPHA.-Keto-.BETA.-allyl-.GAMMA.-butyrolactones. Chem Lett 1991, 1349. <http://dx.doi.org/10.1246/cl.1991.1349>
  • Casiraghi Giovanni, Colombo Lino, Rassu Gloria, Spanu Pietro, Gasparri Fava Giovanna, Ferrari Belicchi Marisa: The four-carbon elongation of three-carbon chiral synthons using 2-(trimethylsiloxy)furan: highly stereocontrolled entry to enantiomerically pure seven-carbon α,β-unsaturated 2,3-dideoxy-aldonolactones. Tetrahedron 1990, 46, 5807. <http://dx.doi.org/10.1016/S0040-4020(01)87777-2>
  • Tochtermann Werner, Schröder Gunter-Rudolf, Snatzke Günther, Peters Eva-maria, Peters Karl, von Schnering Hans Georg: Tetrahydrofurane und Lactone, I. Synthese und Reaktionen chiraler 2,5-überbrückter Tetrahydrofurane – ein neuer Weg zu optisch aktiven γ-Lactonen und γ-Bislactonen. Chem Ber 1988, 121, 1625. <http://dx.doi.org/10.1002/cber.19881210914>
  • Hanessian S., Murray P.J.: Stereochemical control of nature's biosynthetic pathways:A general strategy for the synthesis 0f polypropionate-derived structural units from a single chiral progenitor. Tetrahedron 1987, 43, 5055. <http://dx.doi.org/10.1016/S0040-4020(01)87683-3>