✦ LIBER ✦

Photochemical Investigations. VII. The Photolysis of Unsymmetrical Dimethylhydrazine 1

✍ Scribed by Overman, Joseph D.; Wiig, Edwin O.

Book ID: 126298278
Publisher: American Chemical Society
Year: 1946
Tongue: English
Weight: 297 KB
Volume: 68
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01206a049

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Photochemical Investigations. VIII. The

Photochemical Investigations. VIII. The Photolysis of Solutions of Ethylene Iodide 1

✍ Grabenstetter, Robert J.; Wiig, Edwin O. 📂 Article 📅 1947 🏛 American Chemical Society 🌐 English ⚖ 611 KB

Experimental investigations of the soil

Experimental investigations of the soil buffer capacity relative to the unsymmetrical dimethylhydrazine-induced impact

✍ Krechetov, P. P.; Kasimov, N. S.; Koroleva, T. V.; Chernitsova, O. V. 📂 Article 📅 2014 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 918 KB

Effects of 1,1-unsymmetrical dimethylhyd

Effects of 1,1-unsymmetrical dimethylhydrazine on the murine mixed lymphocyte reaction

✍ D. Jacobs; M.J. Tarr; R.G. Olsen 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 87 KB

Investigation of the alkylating action o

Investigation of the alkylating action of 1,1-dimethylhydrazine

✍ F.W. Krüger; M. Wiessler; U. Rücker 📂 Article 📅 1970 🏛 Elsevier Science 🌐 English ⚖ 79 KB

Investigation of the reaction products o

Investigation of the reaction products of unsymmetrical dimethylhydrazine with potassium permanganate by gas chromatography-mass spectrometry

✍ A. K. Buryak; T. M. Serdyuk; A. V. Ul’yanov 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 149 KB

Photochemical reactions VII [1]. A ‘type

Photochemical reactions VII [1]. A ‘type A rearrangement’ in the photolysis of a steroidal α, β-unsaturated lactone

✍ Vicente Ferrer; José Gómez; Juan-Julio Bonet 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 German ⚖ 220 KB 👁 1 views

## Abstract The irradiation of 17 β‐hydroxy‐2‐oxa‐androst‐4‐en‐3‐one (**1**) yield a cyclopropane derivative **2**, which is the result of a rearrangement, formally analogous to the ‘type A rearrangement’ of the enones. Two other products, the dihydroxy compound **5** and the dimer **6**, have also