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Lederer

The data were extracted from M. Lederer and V. S. Shirley, Table of Isotopes, 7th ed., Wiley-Interscience, New York, 1978 A. H. Wapstra and G. Audi, The 1983 Atomic Mass Evaluation, Nucl. Phys. A432 l-54 (1985) V. S. Shirley, ed.. Table of Radioactive Isotopes, 8th ed., Wiley-Interscience, New York, 1986 and P. Raghavan, Table of Nuclear Moments, At. Data Nucl. Data Tables, 42 189 (1989). [Pg.778]

C. M. Lederer, J. M. HoUander, and I. Perlman, Table of Isotopes, Sixth Edition,John. Wiley Sons, Inc., New York, 1967. [Pg.227]

United States International Trade Commission (USITC), Synthetic Organic Chemicals—United States Production and Sales, 1990, pubhcation 2470, Washington, D.C., Dec. 1991 R. F. Bradley, A. Leder, and Y. Sakuma, Fluorocarbons, ia Chemical Economics Handbook, SRI latematioaal, Menlo Park, Calif., 1990, sections 543.7000—543.7003, plus 1992 supplemental data. [Pg.271]

M. J. Haley with A. Leder and Y. Sakuma, Chemical Economics Handbook, SRI International, Menlo Park, Calif., 1992. [Pg.392]

W. H. Lederer and R. J. Pensterheim, eds.. Arsenic Industrial, Biomedical, Environmental Perspectives, Van Nostrand Reinhold Co., Inc., N.Y., 1983. R. Reddy, ed. Arsenic Metallurgy-Fundamental and Applications, The Metallurgical Society (AIME), Warrendale, Pa., 1988. [Pg.330]

Lederer, F., et al. Improvement of the 2.5 A resolution model of cytochrome bsea by redetermining the primary stmcture and using molecular graphics. [Pg.46]

Spath and Lederer have published a simplified synthesis of harmaline consisting in treating the acetyl derivative of 6-methoxytryptamine (XXIX) with phosphorus pentoxide in boiling xylene, the harmaline thus produced being converted into harmine by catalytic dehydrogenation at 200°. [Pg.495]


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