Conformational control of enolate geometry: a short synthesis of germacrene-DStuart L. Schreiber(Yale University), Ronald C. Hawley(Yale University)Tetrahedron LettersJanuary 1, 198510.1016/s0040-4039(00)98274-1Cited by 32SaveCiteExport RISWatch citationsAbstractRelated PapersRapid chromatographic technique for preparative separations with moderate resolutionW. Clark Still, Michaël Kahn, Abhijit Mitra|The Journal of Organic Chemistry|1978|5.8kHighly selective, kinetically controlled enolate formation using lithium dialkylamides in the presence of trimethylchlorosilaneE. J. Corey, Andrew W. Gross|Tetrahedron Letters|1984|305A method for the regiospecific synthesis of enol triflates by enolate trappingJohn E. Mc Murry, William J. Scott|Tetrahedron Letters|1983|284Germacrene D, a key intermediate of cadinene group compounds and bourbonenesKazuo Yoshihara, Yoshimoto Ohta, Tsutomu Sakai et al.|Tetrahedron Letters|1969|125A new method of olefin synthesis. Coupling of lithium dialkylcuprates with enol triflatesJohn E. McMurry, William J. Scott|Tetrahedron Letters|1980|100