✦ LIBER ✦

ChemInform Abstract: Highly Stereoselective Introduction of Nitrogen Functional Groups into Carbon Frameworks

✍ Scribed by O. TAMURA

Publisher: John Wiley and Sons
Year: 2010
Weight: 26 KB
Volume: 28
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199719274

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective Introduction of Fluorine-Containing Methyl Groups at 2 Position of D-Glucose.

✍ S. HIRAOKA; T. YAMAZAKI; T. KITAZUME 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: Direct Substitution

ChemInform Abstract: Direct Substitution of the Hydroxy Group with Highly Functionalized Nitrogen Nucleophiles Catalyzed by Au(III).

✍ Takashi Ohshima; Yasuhito Nakahara; Junji Ipposhi; Yoshiki Miyamoto; Kazushi Mas 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 63 KB 👁 1 views

ChemInform Abstract: Highly Functional G

ChemInform Abstract: Highly Functional Group Tolerance in Copper-Catalyzed N-Arylation of Nitrogen-Containing Heterocycles under Mild Conditions.

✍ Liangbo Zhu; Gaocan Li; Liang Luo; Peng Guo; Jingbo Lan; Jingsong You 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective Carbon-Functionalization of Electron-Deficient Arylalkenes by Use of Organosilicon Compounds via Photoinduced Electron Transfer.

✍ Tomoo Hayamizu; Hajime Maeda; Munehiro Ikeda; Kazuhiko Mizuno 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

ChemInform Abstract: Heterodimerization

ChemInform Abstract: Heterodimerization of Propylene and Vinylarenes: Functional Group Compatibility in a Highly Efficient Ni-Catalyzed Carbon—Carbon Bond-Forming Reaction.

✍ Jian Jin; T. V. RanjanBabu 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

ChemInform Abstract: ortho-Directed Lith

ChemInform Abstract: ortho-Directed Lithiation Studies of 4-Chloropicolinanilide: Introduction of Functional Groups at C-3 and Their Elaboration to Chain Extended Derivatives via Carbon—Carbon Bond Formation.

✍ M. V. N. DE SOUZA; R. H. DODD 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB

ortho-Directed Lithiation Studies of 4-Chloropicolinanilide: Introduction of Functional Groups at C-3 and Their Elaboration to Chain Extended Derivatives via Carbon-Carbon Bond Formation. -4-Chloropicolinamide (III), prepared by an optimized procedure from picolinic acid (I), undergoes selective LD