✦ LIBER ✦

ChemInform Abstract: Unsaturated Dodecahedranes - Synthesis of the Highly Pyramidalized, Highly Reactive C20H18 and C20H16 Olefins

✍ Scribed by J.-P. MELDER; K. WEBER; A. WEILER; E. SACKERS; H. FRITZ; D. HUNKLER; H. PRINZBACH

Publisher: John Wiley and Sons
Year: 2010
Weight: 26 KB
Volume: 28
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199709274

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Unsaturated Dodecahedranes—In Quest of t

Unsaturated Dodecahedranes—In Quest of the C20H14 1,4,16-Triene and C20H12 1,4,10(14),16-Tetraene, and Their Cations and Anions

✍ Jens Reinbold; Emmerich Sackers; Thomas Oßwald; Klaus Weber; Andreas Weiler; Tor 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 501 KB

The highly pyramidal, highly strained C 20 H 14 1,4,16-dodecahedratriene (4) and C 20 H 12 1,4,10( 14),16-dodecahedratetraene (5) are cage olefins with an intriguing ™inner life∫. For 5 DFT calculations give information about the energetic and geometrical consequences of one-/two-electron oxidation

ChemInform Abstract: Unsaturated Nitrile

ChemInform Abstract: Unsaturated Nitriles: A Domino Ozonolysis-Aldol Synthesis of Highly Reactive Oxonitriles.

✍ F. F. FLEMING; A. HUANG; V. A. SHARIEF; Y. PU 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

ChemInform Abstract: A Highly Conjunctiv

ChemInform Abstract: A Highly Conjunctive β-Keto Phosphonate: Application to the Synthesis of Pyridine Alkaloids Xestamines C, E, and H.

✍ Matthieu Corbet; Michiel de Greef; Samir Z. Zard 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 43 KB

ChemInform Abstract: Heterodimerization

ChemInform Abstract: Heterodimerization of Olefins: A Highly Promising Strategy for the Selective Synthesis of Functionalized Alkenes

✍ Lukas J. Goossen; Nuria Rodriguez 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 15 KB 👁 2 views

ChemInform Abstract: The Synthesis of Hi

ChemInform Abstract: The Synthesis of Highly Reactive, Multi-Functional α,β-Epoxy- and α-Acetoxy-nitrosamines.

✍ M. PARK; F. GU; R. N. LOEPPKY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

ChemInform Abstract: Formation of Bromoc

ChemInform Abstract: Formation of Bromocarbenium Bromide Ion Pairs in the Electrophilic Bromination of Highly Reactive Olefins in Chlorinated Aprotic Solvents.

✍ G. BELLUCCI; C. CHIAPPE; G. LO MORO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Formation of Bromocarbenium Bromide Ion Pairs in the Electrophilic Bromination of Highly Reactive Olefins in Chlorinated Aprotic Solvents. -Kinetic and product distribution data indicate that the bromination of stilbene derivatives with tetrabutylammonium tribromide proceeds via formation of bromoc