Collect. Czech. Chem. Commun.
2000, 65, 524-538
https://doi.org/10.1135/cccc20000524
Versatile Enantioselective Synthesis of Four Diastereomers of Serricornin, a Sex Pheromone of the Cigarette Beetle, Using the SAMP/RAMP-Hydrazone Method
Andreas Job, René Nagelsdiek and Dieter Enders*
Institut für Organische Chemie, Rheinisch-Westfälische Technische Hochschule, Professor-Pirlet-Strasse 1, D-52074 Aachen, Germany
Crossref Cited-by Linking
- Ward Dale E.: The thiopyran route to polypropionates. Chem Commn 2011, 47, 11375. <https://doi.org/10.1039/c1cc13323c>
- Lazny Ryszard, Nodzewska Aneta: N,N-Dialkylhydrazones in Organic Synthesis. From Simple N,N-Dimethylhydrazones to Supported Chiral Auxiliaries. Chem. Rev. 2010, 110, 1386. <https://doi.org/10.1021/cr900067y>
- Enders Dieter, Dhulut Sylvie, Steinbusch Daniel, Herrbach Audrey: Asymmetric Total Synthesis of (−)‐Pironetin Employing the SAMP/RAMP Hydrazone Methodology. Chemistry A European J 2007, 13, 3942. <https://doi.org/10.1002/chem.200601672>
- Enders Dieter, Gries Jörg, Kim Zin‐Sig: Asymmetric Synthesis of 2‐Mono‐ and 2,3‐trans‐Disubstituted Azetidines. Eur J Org Chem 2004, 2004, 4471. <https://doi.org/10.1002/ejoc.200400473>
- Job Andreas, Janeck Carsten F., Bettray Wolfgang, Peters René, Enders Dieter: The SAMP-/RAMP-hydrazone methodology in asymmetric synthesis. Tetrahedron 2002, 58, 2253. <https://doi.org/10.1016/S0040-4020(02)00080-7>
- Salgado Antonio, Boeykens Mark, Gauthier Christine, Declercq Jean-Paul, De Kimpe Norbert: Synthesis of 4-alkyl-1-benzhydryl-2-(methoxymethyl)azetidin-3-ols by regio- and stereoselective alkylation of 1-benzhydryl-3-(N-alkyl)imino-2-(methoxymethyl)azetidine. Tetrahedron 2002, 58, 2763. <https://doi.org/10.1016/S0040-4020(02)00178-3>
- Job Andreas, Nagelsdiek Rene, Enders Dieter: ChemInform Abstract: Versatile Enantioselective Synthesis of Four Diastereomers of Serricornin, a Sex Pheromone of the Cigarette Beetle, Using the SAMP/RAMP‐Hydrazone Method. ChemInform 2000, 31. <https://doi.org/10.1002/chin.200039218>
