✦ LIBER ✦

Endo—Endo Mode lntramolecular Reductive Cyclization of Cyclic 1,2-Bis(silylethynyl)benzenes.

✍ Scribed by Shigehiro Yamaguchi; Masataka Miyasato; Kohei Tamao

Book ID: 101952735
Publisher: John Wiley and Sons
Year: 2004
Weight: 127 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200418182

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: 5-endo-trig Radical

ChemInform Abstract: 5-endo-trig Radical Cyclization of 2-Chloro- and 2,2-Bis(phenylthio)-N-methyl-N-(6-phenylcyclohex-1-en-1-yl)acetamides.

✍ M. IKEDA; S. OHTANI; M. OKADA; E. MINAKUCHI; T. SATO; H. ISHIBASHI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Synthesis of Tetrah

ChemInform Abstract: Synthesis of Tetrahydro-1-benzazocin-2(1H)-ones Using 8-endo-trig Radical Cyclization of 2,2-Bis-(phenylthio)-N-(o-(prop-2-enyl)phenyl) acetamides.

✍ M. IKEDA; K. OBATA; J. OKA; H. ISHIBASHI; T. SATO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Endo and exo phenylene-bridged hetero (O

Endo and exo phenylene-bridged hetero (O,S) silacrown ether rotors including an unexpected structural example of the chloromethyl exchange rule for 1,4-bis(X2methylsilyl)- benzene, XCl, Me

✍ Alejandro J. Metta-Magana; Diana G. Vargas-Pineda; Carlos A. Martinez-Perez; Mar 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 286 KB 👁 1 views

ChemInform Abstract: Syntheses with Perf

ChemInform Abstract: Syntheses with Perfluoroalkyl Iodides. Part 2. Addition to Non-Conjugated Alkadienes; Cyclization of 1,6-Heptadiene and of 4-Substituted 1,6-Heptadienoic Compounds: Bis-allyl Ether, Ethyl Diallylmalonate, N,N′-Diallylamine and N-Substituted Diallylamines; and Additions to Homologous exo- and endo-Cyclic Alkenes, and to Bicyclic Alkenes

✍ Neal O. Brace 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Structure of (bicyclo[2.2.1]hepta-2,5-di

Structure of (bicyclo[2.2.1]hepta-2,5-diene)[(−)-(R,R)-2-exo,3-endo-bis(diphenylphosphino)bicyclo[2.2.1]heptane]rhodium(I) perchlorate tetrahydrofuran solvate, C38H38P2Rh+.ClO4−.C4H8O, the penultimate catalyst precursor in asymmetric reductions using the norphos ligand

✍ Davis, R. E. ;Meyer, B. B. ;Hassett, K. L. ;Juri, P. N. ;Kyba, E. P. 📂 Article 📅 1984 🏛 International Union of Crystallography 🌐 English ⚖ 464 KB