𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Addition of α-Halocarboxylic Acid Esters to para-Substituted Benzaldehydes in the Presence of Pentacarbonyliron.

✍ Scribed by A. B. Terent'ev; T. T. Vasil'eva; N. A. Kuz'mina; N. E. Mysova; O. V. Chakhovskaya

Publisher
John Wiley and Sons
Year
2010
Weight
32 KB
Volume
33
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Addition of Thiols
ChemInform Abstract: Addition of Thiols to α,β-Unsaturated Esters in the Presence of Alumina.
✍ Yoshitada Suzuki; Goroh Saitoh; Satoru Nawa; Mitsuo Kodomari 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Addition of Thiols to α,β-Unsaturated Esters in the Presence of Alumina. -Michael-type additions of thiols to α,β-unsaturated esters in the presence of neutral alumina proceed easily under appropriate mild conditions to give the corresponding adducts [cf. (III), (VI)/(VII)] in good to excellent yie

ChemInform Abstract: Enantioselective Ad
ChemInform Abstract: Enantioselective Addition of Diethylzinc to Benzaldehyde in the Presence of Sulfur-Containing Pyridine Ligands.
✍ G. CHELUCCI; D. BERTA; D. FABBRI; G. A. PINNA; A. SABA; F. ULGHERI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Enantioselective Addition of Diethylzinc to Benzaldehyde in the Presence of Sulfur-Containing Pyridine Ligands. -In some cases ligands, which differ only in the C-8 carbon configuration, cf. methods B) and E), give the opposite configuration of phenylpropanol (III). Surprisingly, method C) leads to

ChemInform Abstract: Asymmetric 1,4 Addi
ChemInform Abstract: Asymmetric 1,4 Addition of Grignard Reagents to Chiral α,β-Unsaturated Esters in the Presence of Lewis Acids.
✍ Giuliana Cardillo; Luca Gentilucci; Alessandra Tolomelli; Claudia Tomasini 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Asymmetric 1,4 Addition of Grignard Reagents to Chiral α,β-Unsaturated Esters in the Presence of Lewis Acids. -The reaction proceeds with good yields but variable diastereoselectivities, depending on the organometallic reagent and Lewis acid used. -(CARDILLO, GIULIANA;

ChemInform Abstract: Reformatsky-Type Ad
ChemInform Abstract: Reformatsky-Type Addition of Esters of α-Halogeno Carboxylic Acids to Aldehydes and Ketones in the Presence of Fe(CO)5.
✍ A. B. Terent'ev; T. T. Vasil'eva; N. A. Kuz'mina; E. I. Mysov; N. S. Ikonnikov; 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

Reformatsky-Type Addition of Esters of α-Halogeno Carboxylic Acids to Aldehydes and Ketones in the Presence of Fe(CO) 5 . -Fe(CO) 5 -promoted Reformatsky-type addition of α-halogenocarboxylates to carbonyl compounds affords the corresponding β-hydroxycarboxylates (III) (12 examples) in moderate to