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Selective Hydrogenations of 1,1-Disubstituted Cyclopropanes

✍ Scribed by Dipl.-Chem. Claus Gröger; Prof. Dr. Hans Musso


Publisher
John Wiley and Sons
Year
1976
Tongue
English
Weight
259 KB
Volume
15
Category
Article
ISSN
0044-8249

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📜 SIMILAR VOLUMES


A New Route to 1,1-Disubstituted Cyclopr
✍ Doz. Dr. J. Gosselck; Dipl.-Chem. G. Schmidt 📂 Article 📅 1968 🏛 John Wiley and Sons 🌐 English ⚖ 211 KB 👁 2 views

polar additions or substitutions [71 induced us t o test the wider use of organotin deuterides for deuteration. Using powerful catalysts such as Raney nickel, palladium, platinum [El, or anhydrous ZnClz (91, we obtained both Cdeuterated and C,U-bisdeuterated alcohols smoothly from organotin deuteri

Calculations on the Polymerization Proce
✍ Daniel Peeters; Georges Leroy 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 207 KB 👁 1 views

Ab initio calculations on the initial steps of the and CH 3 q (q = +, 0, -). Transition structures and energy barriers are obtained for all species, allowing discussion of polymerization process of 1,1-dicyano-, -difluoro-and -dimethyl-substituted cyclopropanes are presented. Polyme-the reaction mec

Asymmetric Hydroboration of 1,1-Disubsti
✍ Stephen P. Thomas; Varinder K. Aggarwal 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 262 KB 👁 2 views

## Abstract **A breakthrough** in the asymmetric hydroboration of notoriously difficult 1,1‐disubstituted alkenes using a new family of highly effective hydroboration reagents is described (see scheme). The intermediate boranes can be oxidized to alcohols or used in Suzuki–Miyaura cross‐coupling re