✦ LIBER ✦

The Chiral Diamine Mediated Asymmetric Baylis–Hillman Reaction

✍ Scribed by Yujiro Hayashi; Tomohiro Tamura; Mitsuru Shoji

Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 117 KB
Volume: 346
Category: Article
ISSN: 1615-4150
DOI: 10.1002/adsc.200404069

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

A chiral diamine, easily prepared from proline, is an effective, asymmetric organic catalyst for the Baylis–Hillman reaction of aldehydes and methyl vinyl ketone, affording adducts with enantioselectivities up to 75%.

📜 SIMILAR VOLUMES

The Asymmetric Baylis—Hillman Reaction

✍ Peter Langer 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 78 KB 👁 1 views

Chiral Lewis Acid Catalyzed Asymmetric B

Chiral Lewis Acid Catalyzed Asymmetric Baylis—Hillman Reactions.

✍ Kung-Shuo Yang; Wei-Der Lee; Jia-Fu Pan; Kwunmin Chen 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

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

Asymmetric Baylis—Hillman Reactions Prom

Asymmetric Baylis—Hillman Reactions Promoted by Chiral Imidazolines.

✍ Junye Xu; Yanyi Guan; Shihui Yang; Yurui Ng; Guangrong Peh; Choon-Hong Tan 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

ChemInform Abstract: The Asymmetric Bayl

ChemInform Abstract: The Asymmetric Baylis—Hillman Reaction.

✍ L. J. BRZEZINSKI; S. RAFEL; J. W. LEAHY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

ChemInform Abstract: Privileged Chiral C

ChemInform Abstract: Privileged Chiral Catalysts in Asymmetric Morita—Baylis—Hillman/Aza-Morita—Baylis—Hillman Reaction

✍ Yin Wei; Min Shi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 20 KB 👁 2 views

Asymmetric Morita—Baylis—Hillman Reactio

Asymmetric Morita—Baylis—Hillman Reactions Catalyzed by Chiral Broensted Acids.

✍ Nolan T. McDougal; Scott E. Schaus 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 114 KB 👁 1 views