✦ LIBER ✦

Comparative mutagenic activity of epoxides derived from 1,3-butadiene

✍ Scribed by C. de Meester; M. Mercier; F. Poncelet

Book ID: 113250377
Publisher: Elsevier Science
Year: 1982
Tongue: English
Weight: 56 KB
Volume: 97
Category: Article
ISSN: 0165-1161
DOI: 10.1016/0165-1161(82)90134-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutagenic activity of vinyl compounds an

Mutagenic activity of vinyl compounds and derived epoxides

✍ Vincent F. Simmon; Jeffrey M. Baden 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 254 KB

Comparative activity of highly mutagenic

Comparative activity of highly mutagenic derivatives of dipyrido[1,2-a:2′,3′-d]imidazoles

✍ K. N'Goy; B. Loukakou; C. N'Zouzi; G. Saint-Ruf; C. de Meester 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 73 KB

High Concentrations of Butadiene Epoxide

High Concentrations of Butadiene Epoxides in Livers and Lungs of Mice Compared to Rats Exposed to 1,3-Butadiene

✍ M.W. Himmelstein; B. Asgharian; J.A. Bond 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 752 KB

Activity and Characterization of Self-Su

Activity and Characterization of Self-Supported Model Catalysts Derived from Cobalt-Based Clusters of Clusters: Hydrogenation of 1,3-Butadiene

✍ M.A. Banares; L. Dauphin; V. Calvoperez; T.P. Fehlner; E.E. Wolf 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 961 KB

Structure activity relationship of epoxi

Structure activity relationship of epoxides: Different mutagenicity of the two diastereoisomeric 3-bromo-1,2-epoxycyclohexanes

✍ G. Bellucci; A. Lippi; F. Marioni; L. Citti; P.G. Gervasi; G. Turchi 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 751 KB

A five step synthesis of (d,l)-estrane d

A five step synthesis of (d,l)-estrane derivatives from 1,3-butadiene

✍ Pierre- Yves Michellys; Hélène Pellissier; Maurice Santelli 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 234 KB

A spidamne 2. obtained in two steps from 1.3-butadiene (ca 50 Q). was metho~ycdonylated GHMDS I dimethykarbonate) and akylated wilh idobenzoc+butene (K2CO3 / acetone) to give 8. Heating of I3 kd to the esuane derivative 9 with 6 contnAled centers. The overall yield from I .3-butediene was ca. 32 46.