✦ LIBER ✦

Oxidation of methylated tetrahydropterins: Structure of the intial quinonoid-dihydropterin intermediate

✍ Scribed by Deniz Ege-Serpkenci; R. Raghavan; Glenn Dryhurst

Publisher: Elsevier Science
Year: 1983
Tongue: English
Weight: 977 KB
Volume: 10
Category: Article
ISSN: 1567-5394
DOI: 10.1016/0302-4598(83)80056-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Spectral studies of the interaction of t

Spectral studies of the interaction of the substrate ‘quinonoid’ 6-methyl dihydropterine and the coenzyme NADH used as marker in the dihydropteridine reductase assay

✍ C. van der Heiden; W. Brink 📂 Article 📅 1982 🏛 Springer 🌐 English ⚖ 540 KB

Spectroscopic observation of the interme

Spectroscopic observation of the intermediates in the oxidation of methyl benzenes

✍ A. Bewick; G.J. Edwards; J.M. Mellor 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 203 KB

The mechanism of oxidation of 6-methyl-5

The mechanism of oxidation of 6-methyl-5-carba-5-deazatetrahydropterin. Evidence for the involvement cf a 4a-adduct in the oxidation of tetrahydropterins.

✍ Graeme Moad; Connie L. Luthy; Stephen J. Benkovic 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 233 KB

Synthesis of Proposed Oxidation—Cyclizat

Synthesis of Proposed Oxidation—Cyclization—Methylation Intermediates of the Coumarin Antibiotic Biosynthetic Pathway.

✍ Junhua Tao; Shanghui Hu; Michelle Pacholec; Christopher T. Walsh 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 125 KB

On the crystal structures of the fluorit

On the crystal structures of the fluorite-related intermediate rare-earth oxides

✍ Peter Kunzmann; LeRoy Eyring 📂 Article 📅 1975 🏛 Elsevier Science 🌐 English ⚖ 619 KB

The mechanism of oxidation of arylpropen

The mechanism of oxidation of arylpropenes to arylpropenals by 2,3-dichloro-5,6-dicyanoquinone: structure of the intermediate

✍ Frank E. Lutz; Edgar F. Kiefer 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 190 KB

In 1968, we reported that l-and 3-arylpropanes were readily oxidized by DDQ to give reactive intermediates which could be directly converted to a variety of products. 1 Shortly thereafter, Sadler and Stewart2 described the conversion of several arylpropenes to aldehydes by excess DDQ. In this repor