✦ LIBER ✦

ChemInform Abstract: N-Alkylation of Tosylamides Using Esters as Primary and Tertiary Alkyl Sources: Mediated by Hydrosilanes Activated by a Ruthenium Catalyst.

✍ Scribed by Takashi Nishikata; Hideo Nagashima

Book ID: 115552952
Publisher: John Wiley and Sons
Year: 2012
Weight: 44 KB
Volume: 43
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201240038

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

N Alkylation of Tosylamides Using Esters

N Alkylation of Tosylamides Using Esters as Primary and Tertiary Alkyl Sources: Mediated by Hydrosilanes Activated by a Ruthenium Catalyst

✍ Dr. Takashi Nishikata; Prof. Dr. Hideo Nagashima 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 465 KB

N Alkylation of Tosylamides Using Esters

N Alkylation of Tosylamides Using Esters as Primary and Tertiary Alkyl Sources: Mediated by Hydrosilanes Activated by a Ruthenium Catalyst

✍ Dr. Takashi Nishikata; Prof. Dr. Hideo Nagashima 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 476 KB

ChemInform Abstract: Hydrosilanes Are no

ChemInform Abstract: Hydrosilanes Are not Always a Reducing Reagent: A Ruthenium-Catalyzed Introduction of Primary Alkyl Groups to Electron-Rich Aromatic Rings Using Esters as a Source of the Alkyl Groups.

✍ Hideo Nagashima; Yuichi Kubo; Mitsunobu Kawamura; Takashi Nishikata; Yukihiro Mo 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 45 KB 👁 1 views

## Abstract Although it is limited to electron‐rich aromatic compounds, the combination of a hydrosilane, an ester, and the ruthenium cluster provides a good method to introduce a primary alkyl group to the aromatic compound.

ChemInform Abstract: Impregnated Rutheni

ChemInform Abstract: Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process.

✍ Rafael Cano; Diego J. Ramon; Miguel Yus 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 63 KB 👁 1 views