✦ LIBER ✦

Gold- and Platinum-Catalyzed Cycloisomerization of Enynyl Esters versus Allenenyl Esters: An Experimental and Theoretical Study

✍ Scribed by Nicolas Marion; Gilles Lemière; Andrea Correa; Chiara Costabile; Rubén S. Ramón; Xavier Moreau; Pierre de Frémont; Rim Dahmane; Alexandra Hours; Denis Lesage; Jean-Claude Tabet; Jean-Philippe Goddard; Vincent Gandon; Luigi Cavallo; Louis Fensterbank; Max Malacria; Steven P. Nolan

Book ID: 102796096
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 536 KB
Volume: 15
Category: Article
ISSN: 0947-6539
DOI: 10.1002/chem.200801387

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Role of Water in Platinum-Catalyzed

The Role of Water in Platinum-Catalyzed Cycloisomerization of 1,6-Enynes: A Combined Experimental and Theoretical Gas Phase Study

✍ Sigrid Baumgarten; Denis Lesage; Vincent Gandon; Jean-Philippe Goddard; Max Mala 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 573 KB

An Experimental and Theoretical Study of

An Experimental and Theoretical Study of the Mechanism of Stannylcupration of α,β-Acetylenic Ketones and Esters

✍ Mårten Ahlquist; Thomas E. Nielsen; Sebastian Le Quement; David Tanner; Per-Ola 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 354 KB 👁 1 views

Mechanism of the Dehydrogenative Silylat

Mechanism of the Dehydrogenative Silylation of Alcohols Catalyzed by Cationic Gold Complexes: An Experimental and Theoretical Study

✍ Stéphanie Labouille; Aurélie Escalle-Lewis; Prof. Yves Jean; Dr. Nicolas Mézaill 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 497 KB 👁 2 views

Pyridine-Catalyzed Stereoselective Addit

Pyridine-Catalyzed Stereoselective Addition of Acyclic 1,2-Diones to Acetylenic Esters: Synthetic and Theoretical Studies of an Unprecedented Rearrangement

✍ Abhilash N. Pillai; Cherumuttathu H. Suresh; Vijay Nair 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 825 KB

## Abstract A systematic study of the addition of various 1,2‐acyclic diones to activated acetylenic esters catalyzed by pyridine under mild conditions is described. This reaction provides a new protocol for the stereoselective synthesis of 1,2‐diaroyl maleates. The exclusive formation of the __cis

3-Bromozinc Propenyl Esters: An Experime

3-Bromozinc Propenyl Esters: An Experimental and Theoretical Study of the Unique Stereocrossover Observed in Their Addition to Aromatic and Aliphatic Aldehydes

✍ Bottoni, A.; Lombardo, M.; Miscione, G. P.; Pujol Algué, J. B.; Trombini, C. 📂 Article 📅 2008 🏛 American Chemical Society 🌐 English ⚖ 438 KB

Michael Addition of Stannyl Ketone Enola

Michael Addition of Stannyl Ketone Enolate to α,β-Unsaturated Esters Catalyzed by Tetrabutylammonium Bromide and an ab initio Theoretical Study of the Reaction Course.

✍ Makoto Yasuda; Kouji Chiba; Noriyuki Ohigashi; Yasuhiro Katoh; Akio Baba 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 155 KB

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