✦ LIBER ✦

Radical addition of t-butyl mercaptan to 1,2,3,4,7,7 hexamethylbicyclo[2.2.1]heptadiene

✍ Scribed by E.N Prilezhaeva; V.A Asovskaya; G.U Stepanyanz; D Mondeshka; R.J Shekhtman

Publisher: Elsevier Science
Year: 1969
Tongue: French
Weight: 196 KB
Volume: 10
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)88844-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: 2-Azabicyclo[2.2.1]

ChemInform Abstract: 2-Azabicyclo[2.2.1]hept-5-enes from 7-Azabicyclo[2.2.1]heptadienes by Tandem Intermolecular Radical Addition—Homoallylic Radical Rearrangement.

✍ David M. Hodgson; Magnus W. P. Bebbington; Paul Willis 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Reactions of 2,3-dicarbomethoxy-7-oxabic

Reactions of 2,3-dicarbomethoxy-7-oxabicyclo[2.2.1]heptadiene with molybdenum carbonyls

✍ Chia-Hsing Sun; Tahsin J. Chow 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 251 KB

2,2,4,4-Tetra-tert-butyl-1,3,5,2,4-benzo

2,2,4,4-Tetra-tert-butyl-1,3,5,2,4-benzotrioxadisilepine-7-carbaldehyde

✍ L. C. R. Andrade; J. A. Paixao; M. J. M. de Almeida; C. Siquet; F. Borges 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 10 KB 👁 1 views

Regioselective Radical Additions to 7-Ox

Regioselective Radical Additions to 7-Oxabicyclo[2.2.1]hept-5-en-2-one

✍ Jean-Paul Vionnet; Kurt Schenk; Philippe Renaud 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 German ⚖ 658 KB

## Abstract Radical addition to 7‐oxabicylco[2.2.1]hept‐5‐en‐2‐one (1) was examined from a regiochemical point of view, and despite the small electronic anisotropy of the double bond, electrophilic radicals were found to add preferentially at C(5) with selectivities of up to 5:1. We also report the

ChemInform Abstract: Preparation of Ster

ChemInform Abstract: Preparation of Sterically Congested Compounds: 6,7-Di-t-butyl-1,4-naphthoquinone, 2,3,6,7-Tetra-t-butylanthraquinone, and 2,3,6,7-Tetra-t-butylanthracene.

✍ Kazuki Iguchi; Yoshiaki Sugihara; Juzo Nakayama 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Addition of radicals to quinones—IV. ESR

Addition of radicals to quinones—IV. ESR study of some radical reactions of 2,6-di-t. butyl-1,4-benzoquinone

✍ T.L. Simándi; A. Rockenbauer 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 302 KB

The radical reactions of 2,6-di-t. butyl-1,4-benzoquinone with various thermally decomposing azocompounds and peroxides have been studied by ESR. On the basis of the ESR spectra of the intermediate radicals, the mechanism of the reaction is suggested. It was found that, while primary alkyl radicals