gon for the phenyl group with d(C,C) = 1.39, tf(C,H) = 1.08, rf(Ci,C7) = 1.40, d(C7,0) = 1.21 Ã, and ct(Ci,C7,0) = 120°. 6 The nomenclature cis and ...
2028 J. Org. Chem., Vol. 42, No. 11, 1977. Notes. (12) M. Sanesi and M. Larzarone, Ric. Sci., Parte 2: Sez. A, 2, 138 (1962);. (13) R. Huisgen and V.
Mark Lefever , Jerome W. Kosmeder , II , Michael Farrell , and Christopher Bieniarz .... Donald R. Mills , Fred Russell Kramer , Carl Dobkin , Tohru Nishihara , Patricia E. Cole .... ERNST FREESE , CHINGJU W. SHEU , ENID GALLIERS.
Quantitative addition of bisulfite to uracil and cytosine in hot aqueous solution at pH ~6 produced 5,6- dihydrouracil-6-sulfonate (la). Compound la was obtained.
Department of Chemistry, Bagley Hall, Box 351700, University of Washington, .... FrantiÅ¡ek TureÄek , Jace W. Jones , Tyrell Towle , Subhasis Panja , Steen ...
The Journal of Physical Chemistry B 0 (proofing), ... Journal of the American Chemical Society 2008 130 (44), 14584-14596 ... Adenine Radicals in the Gas Phase: An Experimental and Computational Study of Hydrogen Atom Adducts to ...
May 1, 2002 - This article is cited by 5 publications. Guo-ping Lu, Chun Cai, Fei Chen, Ren-long Ye, and Bao-jing Zhou . Facile Sulfa-Michael Reactions with ...
methylcholanthrene, 9,10-dimethyl-l,2- benzanthracene, perylene, and naph- thacene. It is possible that further study of interactions of this type may offer a clue ...
addition compounds with any of the hydrocarbons ... that it will form addition compounds ..... Armour Industrial Chemical Co., 1355 West 31st St., Chicago 9, III.
the canonical structure. ... canonical form is the most stable. ... perturbative triples [CCSD(T)] method and the modified cc-pVTZ19 basis set lacking f func-.
Buffer Additives for Lime/Limestone Slurry Scrubbing. GARY T. ROCHELLE , WILLIAM T. WEEMS , RAYMOND J. SMITH , and MARY W. HSIANG. 1982,243-265.
724 Table 111. INDO Hyperfine Coupling Constants (G) for the
The Addition of Sodium Bisulfite to Uracil and to Cytosine
Benzoyl Radical" PlanaP cis trans a H ( o r tho) a~tmeta) aH(para) a1acg
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