✦ LIBER ✦

Mechanism of the Addition Reaction of Alkyl Azides to [60]Fullerene and the Subsequent N 2 Extrusion to Form Monoimino-[60]fullerenes

✍ Scribed by Cases, Montserrat; Duran, Miquel; Mestres, Jordi; Martín, Nazario; Solà, Miquel

Book ID: 118005056
Publisher: American Chemical Society
Year: 2001
Tongue: English
Weight: 225 KB
Volume: 66
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo0010431

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 1,2,3,4-Bisiminofullerene a

Synthesis of 1,2,3,4-Bisiminofullerene and 1,2,3,4-Bis(triazolino)fullerene—on the Mechanism of the Addition Reactions of Organic Azides to [60]Fullerene

✍ Clifton K.-F. Shen; Hsiao-Hua Yu; Chiun-Gung Juo; Kuo-Ming Chien; Guor-Rong Her; 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 467 KB 👁 1 views

ChemInform Abstract: Synthesis of 1,2,3,

ChemInform Abstract: Synthesis of 1,2,3,4-Bisiminofullerene and 1,2,3,4-Bis(triazolino) fullerene. Mechanism of the Addition Reactions of Organic Azides to ( 60)Fullerenes.

✍ C. K.-F. SHEN; H. YU; C.-G. JUO; K.-M. CHIEN; G.-R. HER; T.-Y. LUH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

Diels–Alder reaction of [60]fullerene wi

Diels–Alder reaction of [60]fullerene with cyclooctatetraene and electrophilic addition to the cycloadduct

✍ Hiroshi Ishida; Kenichi Komori; Kenji Itoh*; Masatomi Ohno 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 69 KB

60]Fullerene reacted with cyclooctatetraene as a dienic partner in the Diels-Alder reaction to give the 1:1 cycloadduct in satisfactory yield (51%), which was attained by heating at relatively low temperature (110°C) and for an extended period (2 days). The cycloadduct underwent electrophilic additi

ChemInform Abstract: Diels—Alder Reactio

ChemInform Abstract: Diels—Alder Reaction of [60]Fullerene with Cyclooctatetraene and Electrophilic Addition to the Cycloadduct.

✍ Hiroshi Ishida; Kenichi Komori; Kenji Itoh; Masatomi Ohno 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Structural Reassignment of the Mono- and

Structural Reassignment of the Mono- and Bis-Addition Products from the Addition Reactions of N-(Diphenylmethylene)glycinate Esters to [60]Fullerene under Bingel Conditions

✍ Ball, Graham E.; Burley, Glenn A.; Chaker, Leila; Hawkins, Bill C.; Williams, Ja 📂 Article 📅 2005 🏛 American Chemical Society 🌐 English ⚖ 133 KB

Structural Reassignment of the Mono- and

Structural Reassignment of the Mono- and Bis-Addition Products from the Addition Reactions of N-(Diphenylmethylene)glycinate Esters to [60]Fullerene under Bingel Conditions.

✍ Graham E. Ball; Glenn A. Burley; Leila Chaker; Bill C. Hawkins; James R. William 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 8 KB 👁 1 views

Fullerene derivatives Q 1145 Structural Reassignment of the Mono-and Bis-Addition Products from the Addition Reactions of N-(Diphenylmethylene)glycinate Esters to [60]Fullerene under Bingel Conditions. -(BALL, G. E.;