Cobalt-Catalyzed Cross-Coupling Reaction between Functionalized Primary and Secondary Alkyl Halides and Aliphatic Grignard Reagents

ChemInform Abstract: Cobalt-Catalyzed Cr

ChemInform Abstract: Cobalt-Catalyzed Cross-Coupling Reaction Between Functionalized Primary and Secondary Alkyl Halides and Aliphatic Grignard Reagents.

✍ Gerard Cahiez; Christophe Chaboche; Christophe Duplais; Arianna Giulliani; Alban 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 39 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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

Iron-Catalyzed Cross-Coupling of Primary

Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents.

✍ Masaharu Nakamura; Keiko Matsuo; Shingo Ito; Eiichi Nakamura 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 222 KB 👁 1 views

ChemInform Abstract: Nickel-Catalyzed Cr

ChemInform Abstract: Nickel-Catalyzed Cross-Coupling Between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides.

✍ Anne Eeg Jensen; Paul Knochel 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

Cobalt-Catalyzed Coupling Reaction of Al

Cobalt-Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard Reagents

✍ Takashi Tsuji; Hideki Yorimitsu; Koichiro Oshima 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB 👁 2 views

Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbon±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 ±sp, sp 2 ±sp 2 , a

Cobalt-Catalyzed Coupling Reaction of Al

Cobalt-Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard Reagents

✍ Takashi Tsuji; Hideki Yorimitsu; Koichiro Oshima 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB 👁 2 views

Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbon±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 ±sp, sp 2 ±sp 2 , a

Cobalt-Catalyzed Coupling Reaction of Al

Cobalt-Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard Reagents.

✍ Takashi Tsuji; Hideki Yorimitsu; Koichiro Oshima 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 229 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.