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Thermochemistry of adducts of triphenyl derivatives of N, P and As with arsenic trihalides
(Elsevier Science BvAmsterdamHolanda, 1996)
Mechanochemical Synthesis of Urea Adducts with Long Chain Alkyl Derivatives
(Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2013-01-16)
Estimate of Delta(D) H-m(o) for adducts by thermogravimetry.
(Soc Brasileira QuimicaSao PauloBrasil, 1998)
Electrochemical and theoretical evaluation of the interaction between dna and amodiaquine: evidence of the guanine adduct formation
(Sociedade Brasileira de Química, 2010-01-01)
The electrochemical behavior of the interaction of amodiaquine with DNA on a carbon paste electrode was studied using voltametric techniques. In an acid medium, an electroactive adduct is formed when amodiaquine interacts ...
Electrochemical and theoretical evaluation of the interaction between dna and amodiaquine: evidence of the guanine adduct formation
(Sociedade Brasileira de Química, 2010-01-01)
The electrochemical behavior of the interaction of amodiaquine with DNA on a carbon paste electrode was studied using voltametric techniques. In an acid medium, an electroactive adduct is formed when amodiaquine interacts ...
Keto-Enol Tautomerism in Passerini and Ugi Adducts
The use of arylglyoxal as starting material in Passerini and Ugi reactions affords β-ketoamides. This has allowed to study keto-enol tautomerism in these systems and assess the way in which the presence of acyloxy or ...
Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA
(AMER CHEMICAL SOC, 2009)
The well established rat hepatocarcinogen N-nitrosopytrolidine (NPYR, 1) requires metabolic activation to DNA adducts to express its carcinogenic activity. Among the NPYR-DNA adducts that have been identified, the cyclic ...
Diterpenic adducts from Xylopia species
(1991-12-01)
Xylopia emarginata and X. amazonica contain diterpene adducts probably originating from Diels-Aider reaction between labdane and kaurane derivatives. This type of substance seems to be characteristic of the genus Xylopia. © 1991.