✦ LIBER ✦

The first Et3N-mediated transesterification of β-keto esters using Baylis–Hillman alcohols

✍ Scribed by Olfa Mhasni; Farhat Rezgui

Book ID: 108283622
Publisher: Elsevier Science
Year: 2011
Tongue: French
Weight: 685 KB
Volume: 67
Category: Article
ISSN: 0040-4020
DOI: 10.1016/j.tet.2011.06.012

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: The First Et3N-Medi

ChemInform Abstract: The First Et3N-Mediated Transesterification of β-Keto Esters Using Baylis—Hillman Alcohols.

✍ Olfa Mhasni; Farhat Rezgui 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 36 KB

## Abstract Title reaction provides access to a variety of allylic esters (III) and (V) in moderate to good yields.

THE BAYLIS—HILLMAN REACTION: TiCl 4 MEDI

THE BAYLIS—HILLMAN REACTION: TiCl 4 MEDIATED COUPLING OF ALKYL VINYL KETONES WITH α-KETO ESTERS AND ALDEHYDES

✍ Basavaiah, Deevi; Sreenivasulu, Bandaru; Reddy, Ravi Mallikarjuna; Muthukumaran, 📂 Article 📅 2001 🏛 Taylor and Francis Group 🌐 English ⚖ 172 KB

ChemInform Abstract: The Baylis—Hillman

ChemInform Abstract: The Baylis—Hillman Reaction: TiCl4 Mediated Coupling of Alkyl Vinyl Ketones with α-Keto Esters and Aldehydes.

✍ Deevi Basavaiah; Bandaru Sreenivasulu; Ravi Mallikarjuna Reddy; Kannan Muthukuma 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

The first DMAP-mediated palladium-free T

The first DMAP-mediated palladium-free Tsuji–Trost-type reaction of cyclic and acyclic Baylis–Hillman alcohols with active methylene compounds

✍ Olfa Mhasni; Farhat Rezgui 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 340 KB

Direct allylic substitution of cyclic Baylis-Hillman alcohols with active methylene compounds under modified Taber's conditions (DMAP, toluene, reflux, 4 Å molecular sieves), with no Pd catalysts/activating agents, as is usually required for the process, affords the C-allylation products in moderate

ChemInform Abstract: The First DMAP-Medi

ChemInform Abstract: The First DMAP-Mediated Palladium-Free Tsuji—Trost-Type Reaction of Cyclic and Acyclic Baylis—Hillman Alcohols with Active Methylene Compounds.

✍ Olfa Mhasni; Farhat Rezgui 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 62 KB 👁 1 views

Enantioselective Synthesis of the Optica

Enantioselective Synthesis of the Optically Active α-Methylene-β-hydroxy Esters, Equivalent Compounds to Morita—Baylis—Hillman Adducts, Using Successive Asymmetric Aldol Reaction and Oxidative Deselenization.

✍ Isamu Shiina; Yu-suke Yamai; Takahisa Shimazaki 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

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