✦ LIBER ✦

Towards Direct Mukaiyama-Type Reactions Catalytic in Silicon

✍ Scribed by Prof. Dr. Jesús M. García; Prof. Dr. Mikel Oiarbide; Prof. Dr. Claudio Palomo

Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 257 KB
Volume: 50
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.201102423

No coin nor oath required. For personal study only.

✦ Synopsis

We thank the Ministerio de Ciencia e Innovación (Spain) (CTQ2010-21263-C02) for financial support.

📜 SIMILAR VOLUMES

ChemInform Abstract: Towards Direct Muka

ChemInform Abstract: Towards Direct Mukaiyama-Type Reactions Catalytic in Silicon

✍ Jesus M. Garcia; Mikel Oiarbide; Claudio Palomo 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

Direct Catalytic Aldol-Type Reactions Us

Direct Catalytic Aldol-Type Reactions Using RCH2CN.

✍ Yutaka Suto; Naoya Kumagai; Shigeki Matsunaga; Motomu Kanai; Masakatsu Shibasaki 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 257 KB

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

Direct Catalytic Asymmetric anti-Selecti

Direct Catalytic Asymmetric anti-Selective Mannich-Type Reactions.

✍ Ismail Ibrahem; Armando Cordova 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

ChemInform Abstract: Direct-Type Vinylog

ChemInform Abstract: Direct-Type Vinylogous Mukaiyama—Michael Addition Reactions Involving Pyrrolinone Donors.

✍ Andrea Sartori; Claudio Curti; Lucia Battistini; Paola Burreddu; Gloria Rassu; G 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Direct-Type Catalytic Three-Component Ma

Direct-Type Catalytic Three-Component Mannich Reaction in Aqueous Media.

✍ Thierry Ollevier; Etienne Nadeau; Andree-Anne Guay-Begin 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 22 KB 👁 1 views

Direct Catalytic Asymmetric Mannich-Type

Direct Catalytic Asymmetric Mannich-Type Reaction of Thioamides

✍ Yuta Suzuki; Ryo Yazaki; Naoya Kumagai; Masakatsu Shibasaki 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 403 KB 👁 1 views

## Abstract **Taking the reins**: The title transformation of thioamides and __N__‐diphenylphosphinoyl imines is described. By harnessing the power of cooperative catalysis between a soft Lewis acid and a hard Brønsted base, thioamide carbon pronucleophiles can furnish Mannich products (see scheme)