1 Potential Anticancer Agents. XV. Synthesis of 9-p - American ...https://pubs.acs.org/doi/pdf/10.1021/jo01106a040by EJ REIST - â1958 - âCited by ...
HEIST,SPENCER. AND BAKER. VOL. 23. Anal. Caled, for CioHgN509S: C, 32.0; H, 2.42; N, 18.7. Found: C, 31.9; H, 2.57; N, 18.5. ir2-Amino-5,6-dihydro-4H-l ...
Long Liu , Cheng-Qian Wang , Dan Liu , Wei-Gang He , Jin-Yi Xu , Ai-Jun Lin , He-Quan Yao , Genzoh Tanabe , Osamu Muraoka , Wei-Jia Xie , and Xiao-Ming ...
Laboratory,1 Southern Research Institute]. Synthesis of Potential Anticancer Agents. XV. Ribonucleosides of 2-Substituted. Purines. By Howard J. Schaeffer and.
Howard J. Schaeffer, H. Jeanette Thomas. J. Am. Chem. Soc. , 1958 ... Hayden Peacock , Olena Maydanovych and Peter A. Beal. Organic Letters 2010 12 (5), ...
and succinimide gave the corresponding nitrogen mustard derivatives. Condensation of ... the pharmacodynamic mustard function selectively to malignant cells ...
this compound an attractive starting material for the preparation of both the bis-mustard and the cor- responding one-armed mustard of 3-amino-3-.
5,5Dimethyl-4-phenyl-2-(3-pyridyl)-A1-pyrroline (11) did not react with phenyl isothiocyanate. When 11 was heated with phthalic anhydride at 210' for. 15 min.
3108. Leonard 0. Ross, Leon Goodman and B. R. Baker. Vol. 81. A suspension of 9.5g. of the above hydrochloride in 50 ml. of water was adjusted to pH 7 with ...
The authors are indebted to. Dr. Peter Lim for interpretation ofthe infrared ... new and useful synthesis of 6-deoxy-l,2-0-isopropylidene-L-idofuranose (IX). The latter was ..... After 36 ml. of 10% aqueous sodium hydroxide was added,. Celite was ...
POTENTIAL ANTICANCER AGENTS. X. 1753 hr. during which air was passed through the mixture. After filtering the hot solution, almost colorless needles, m.p..
1958
VOL.
REIST, SPENCER. AND BAKER
Anal. Calcd. for C10H9N509S:C, 32.0; H, 2.42; N, 18.7. Found: C, 31.9; H, 2.57; N, 18.5. ~2-Aminn-6,6dihydro-~H-l,S-thiazine-~-carboxylic acid (XVIII) was prepared according to the procedure of Schoberl and I