✦ LIBER ✦

Di-tert-Butyl Acetylenedicarboxylate and Its Cyclotrimerization

✍ Scribed by Prof. Dr. Wolfgang Sucrow; Dr. Fritz Lübbe

Publisher: John Wiley and Sons
Year: 1979
Tongue: English
Weight: 222 KB
Volume: 18
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.197901491

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

[2 + 4]-Cycloadditions with Di-tert-buty

[2 + 4]-Cycloadditions with Di-tert-butyl Acetylenedicarboxylate

✍ Gisela Weber; Dr. Klaus Menke; Prof. Dr. Henning Hopf 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 218 KB

Addition and cycloaddition reactions of

Addition and cycloaddition reactions of di-tert-butyl(di-tert-butylphenylsilylimino) silane

✍ Jörg Niesmann; Uwe Klingebiel; Mathias Noltemeyer 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 828 KB

ChemInform Abstract: Di-tert.-butyl Dica

ChemInform Abstract: Di-tert.-butyl Dicarbonate

✍ Stephen A. Lawrence 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 22 KB 👁 2 views

1,3-Di(tert-butyl)-2,4-dichlorodiazadiph

1,3-Di(tert-butyl)-2,4-dichlorodiazadiphosphetidine

✍ Doz. Dr. O. J. Scherer; Dipl.-Chem. P. Klusmann 📂 Article 📅 1969 🏛 John Wiley and Sons 🌐 English ⚖ 216 KB 👁 1 views

2,4-di-tert-butyl- and 2,3,4,5-tetrachlo

2,4-di-tert-butyl- and 2,3,4,5-tetrachloronorcaradiene

✍ Mordecai B. Rubin 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 196 KB

The title norcaradienes have been synthesized by low temperature photolysis and the activation parameters for their isomerization to cycloheptatrienes determined.

ChemInform Abstract: The Reactions of 3,

ChemInform Abstract: The Reactions of 3,6-Di-tert-butyl-1,2-benzoquinone and 3,6-Di-tert-butylcatechol with tert-Butyl Hydroperoxide.

✍ V. N. Glushakova; N. A. Skorodumova; V. I. Nevodchikov; L. G. Abakumova; N. P. M 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

The Reactions of 3,6-Di-tert-butyl-1,2-benzoquinone and 3,6-Ditert-butylcatechol with tert-Butyl Hydroperoxide. -The reaction of the title quinone (I) as well as its corresponding catechol with tert-butyl hydroperoxide in aprotic solvents results in ring oxidation accompanied by ring expansion furn