✦ LIBER ✦

Stereoselective titanium-mediated aldol reactions of α-benzyloxy methyl ketones

✍ Scribed by Miquel Pellicena; Joan G. Solsona; Pedro Romea; Fèlix Urpí

Book ID: 119375803
Publisher: Elsevier Science
Year: 2012
Tongue: French
Weight: 679 KB
Volume: 68
Category: Article
ISSN: 0040-4020
DOI: 10.1016/j.tet.2012.09.096

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1,4-Asymmetric induction in the titanium

1,4-Asymmetric induction in the titanium-mediated aldol reactions of α-benzyloxy methyl ketones

✍ Miquel Pellicena; Joan G. Solsona; Pedro Romea; Fèlix Urpí 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 171 KB

ChemInform Abstract: 1,4-Asymmetric Indu

ChemInform Abstract: 1,4-Asymmetric Induction in the Titanium-Mediated Aldol Reactions of α-Benzyloxy Methyl Ketones.

✍ Miquel Pellicena; Joan G. Solsona; Pedro Romea; Felix Urpi 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective Titanium-Mediated Aldol Reaction from (S)-4-Benzyloxy-3-methyl-2-butanone.

✍ Joana Zambrana; Pedro Romea; Felix Urpi; Cristina Lujan 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 47 KB

Highly stereoselective aldol reactions o

Highly stereoselective aldol reactions of titanium enolates from ethyl α-silyloxyalkyl ketones

✍ Sergi Figueras; Ricardo Martín; Pedro Romea; Fèlix Urpí; Jaume Vilarrasa 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 219 KB

Stereoselective Titanium-Mediated Aldol

Stereoselective Titanium-Mediated Aldol Reactions of a Chiral Lactate-Derived Ethyl Ketone with Ketones

✍ Alcoberro, Sandra; Gómez-Palomino, Alejandro; Solà, Ricard; Romea, Pedro; Urpí, 📂 Article 📅 2013 🏛 American Chemical Society 🌐 English ⚖ 347 KB

1,4-syn-Asymmetric induction in the tita

1,4-syn-Asymmetric induction in the titanium-mediated aldol reactions of chiral methyl α-silyloxy ketones

✍ Adriana Lorente; Miquel Pellicena; Pedro Romea; Fèlix Urpí 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 300 KB

Good levels of 1,4-syn asymmetric induction are obtained in the TiCl 4 -mediated aldol reaction of methyl a-silyloxy ketones with achiral aldehydes. Such methodology represents a new approach to the substrate-controlled acetate aldol reaction, which can be useful to design more efficient syntheses o