Dictionary of Organic Compounds by G. Pattenden, J. I. G. Cadogan, S. V. Ley (auth.)

By G. Pattenden, J. I. G. Cadogan, S. V. Ley (auth.)

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Bp05 108°. 4687. C. et al, Rev. Roum. A. , 1991, 56, 4112 (synth, pmr, cmr, ms) Gryehtol, K. et al, Chem. W. 3 Yellow eryst. Mp 230°. 4 Sm. Pale yellow solid. 8-1-00085 1-Norpinanol [130775-52-9] 7-M ercaptonorbornane. J. et al, Tet. B. E. J. C. , 1990, 55, 4564 (synth, pmr, cmr) Kostova, K. et al, Synth. 1 Waxy needles. Mp 63-65°. 4-Methylbenzenesuljonyl: [13866-80-3]. Cryst. (hexane). Mp 78-80°. Me ether: [61192-27-6]. 2 Liq. L. 5 Ligand for asymmetrie hydrogenation. (2R* ,3R*)-form [79426-29-2] ( + )-endo,exo-form Solid.

Hippurorubrine 5,5' -Bi(I,4,2-dithiazol-5ylidene) 8-1-00103 [72884-72-1] o 5-(1,4,2-Dithiazol-5-ylidene)-1 ,4,2-dithiazole, 9CI N~S PhrNph Sc, l S>==< S~N o (E)-form 11 (dinitrile) Overberger, CG. 3 Obt. as mixt. of E and Z-forms. Electron donor. Red solid. T. 2 (±)-form Obt. from N-Benzoylglyeine, B-0-01282. Red cryst. (diphenyl ether). Mp 305-308° dec. -D. et af, Arch. Pharm. 3 Solid. Mp 213-215°. A. , 1967,32, 1572. 2 (lRS,6RS)-form trans:form Strained 'inside-outside' bicyclo system. Model for ingenane diterpenes.

BtOH). Mp 280-283°. 1 Cryst. (DMF). Mp 280-283°. 2-ß-D-Arabinofuranosyl: [19131-40-9]. 2 Solid. 2-ß-D-Ribofuranosyl: [15147-69-0]. 2 Cryst. Mp 260261° dec. 46 in DMSO). Gut, J. et al, Coll. Czech. Chem. , 1966, 31, 2014 (synth, deriv) Zemlicka, J. el al, Coll. Czech. Chem. J. et al, J. A. el al, J. Het. , 1979, 16, 585 (synth, uv) Beranek, J. et al, Coll. Czech. Chem. 1 Mp 121-122°. S. el al, Heterocycles, 1994,37, 775. 1 Light orange solid. Mp 56-58°. E. et al, J. Med. 1 Mp 154-155°. Strekowski, L.

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