Citation: Jr. Lennox et al., Enantiospecific synthesis of annulated nicotine analogues from D-Glutamic acid. 7-azabicyclo[2.2.1]heptano[2.3-c]pyridines, J ORG CHEM, 66(21), 2001, pp. 7078-7083
Citation: H. Rapoport et S. Rapoport, The Transasia-Corp. 'Leonardo' website dispute continued, message of support for 'Leonardo', LEONARDO, 33(3), 2000, pp. 241-241
Citation: Sc. Turner et al., Enantiospecific synthesis of annulated nicotine analogues from D- and L-glutamic acid. Pyridotropanes, J ORG CHEM, 65(3), 2000, pp. 861-870
Citation: If. Pickersgill et H. Rapoport, Preparation of functionalized, conformationally constrained DTPA analoguesfrom L- or D-serine and trans-4-hydroxy-L-proline. Hydroxymethyl substituents on the central acetic acid and on the backbone, J ORG CHEM, 65(13), 2000, pp. 4048-4057
Citation: Tb. Sim et H. Rapoport, N-trityl- and N-phenylfluorenyl-N-carboxyanhydrides and their use in dipeptide synthesis, J ORG CHEM, 64(7), 1999, pp. 2532-2536
Citation: Bp. Hart et H. Rapoport, Conformationally constrained 7-azabicyclo[2.2.1]heptane amino acids. Synthesis of a glutamic acid analogue, J ORG CHEM, 64(6), 1999, pp. 2050-2056
Citation: Ma. Shalaby et H. Rapoport, A general and efficient route to thionoesters via thionoacyl nitrobenzotriazoles, J ORG CHEM, 64(3), 1999, pp. 1065-1070
Citation: Cr. Hurt et al., Enantiospecific synthesis of (R)-4-amino-5-oxo-1,3,4,5-tetrahydrobenz[cd]indole, an advanced intermediate containing the tricyclic core of the ergots, J ORG CHEM, 64(1), 1999, pp. 225-233