By G. Pattenden, J. I. G. Cadogan, S. V. Ley (auth.)
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Seeing that its unique visual appeal in 1977, complicated natural Chemistry has maintained its position because the most suitable textbook within the box, supplying vast assurance of the constitution, reactivity and synthesis of natural compounds. As within the prior variations, the textual content includes broad references to either the first and overview literature and gives examples of knowledge and reactions that illustrate and record the generalizations.
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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.