✦ LIBER ✦

ChemInform Abstract: Highly Stereoselective Synthesis of syn-1,3-Diols Through a Sequential Titanium-Mediated Aldol Reaction and LiBH4 Reduction.

✍ Scribed by Judit Esteve; Sonia Matas; Miquel Pellicena; Javier Velasco; Pedro Romea; Felix Urpi; Merce Font-Bardia

Publisher: John Wiley and Sons
Year: 2010
Weight: 43 KB
Volume: 41
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201038049

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Titanium-Mediated A

ChemInform Abstract: Titanium-Mediated Aldol-Tishchenko Reaction: A Stereoselective Synthesis of Differentiated anti 1,3-Diol Monoesters.

✍ R. MAHRWALD; B. COSTISELLA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

ChemInform Abstract: TiCl4-Mediated Redu

ChemInform Abstract: TiCl4-Mediated Reduction of 1,3-Diketones with BH3—Pyridine Complex: A Highly Diastereoselective Method for the Synthesis of syn-1,3-Diols.

✍ Giuseppe Bartoli; Marcella Bosco; M. Cristina Bellucci; Renato Dalpozzo; Enrico 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

ChemInform Abstract: Ester Derived Titan

ChemInform Abstract: Ester Derived Titanium Enolate Aldol Reaction: Highly Diastereoselective Synthesis of syn- and anti-Aldols.

✍ A. K. GHOSH; S. FIDANZE; M. ONISHI; K. A. HUSSAIN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

## 1998 hydroxycarboxylic acids hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters P 0280 ## 01 -075 Ester Derived Titanium Enolate Aldol Reaction: Highly Diastereoselective Synthesis of syn-and anti-Aldols. -Titanium enolates derived from esters (I) undergo aldol rea

ChemInform Abstract: A Highly Diastereos

ChemInform Abstract: A Highly Diastereoselective TiCl4-Mediated Reduction of β-Hydroxy Ketones with BH3×Py — A Very Efficient and General Synthesis of syn-1,3-Diols.

✍ Giuseppe Bartoli; Marcella Bosco; Enrico Marcantoni; Massimo Massaccesi; Samuele 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 41 KB 👁 1 views

A Highly Diastereoselective TiCl4-Mediat

A Highly Diastereoselective TiCl4-Mediated Reduction of β-Hydroxy Ketones with BH3·py — A Very Efficient and General Synthesis of syn-1,3-Diols

✍ Giuseppe Bartoli; Marcella Bosco; Enrico Marcantoni; Massimo Massaccesi; Samuele 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 332 KB 👁 1 views

ChemInform Abstract: An Efficient Method

ChemInform Abstract: An Efficient Method for the Synthesis of Enantiopure 2,3-anti-Propionate Aldols Involving a 3,5-syn- or anti-Diol Subunit Through Chiral Borane-Mediated Enantioselective Aldol Reaction Coupled with Radical Reduction.

✍ Syun-ichi Kiyooka; Kazi A. Shahid 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views