✦ LIBER ✦

Enantioselective hydrolysis of cis -1,2-diacetoxycycloalkanedimethanols:enzymatic preparation of chiral building blocks from prochiral meso -substrates.

✍ Scribed by Kurt Laumen; Manfred Schneider

Publisher: Elsevier Science
Year: 1985
Tongue: French
Weight: 236 KB
Volume: 26
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)94782-8

No coin nor oath required. For personal study only.

✦ Synopsis

The enzymatic hydrolysis of the prochiral title compounds in presence of porcine liver esterase (PLE) and lipase from porcine pancreas (PPL) was studied, resulting in the preparation of the chiral monoacetates 12 -r with high (72-998e.e.

📜 SIMILAR VOLUMES

Enzymatic Syntheses of Chiral Building B

Enzymatic Syntheses of Chiral Building Blocks from Prochiral meso-Substrates: Preparation of Methyl(hydrogen)-1,2-cycloalkanedicarboxylates

✍ Prof. Dr. Manfred Schneider; Dr. Norbert Engel; Petra Hönicke; Gerd Heinemann; P 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 217 KB 👁 1 views

Enzymatic Synthesis of Chiral Building B

Enzymatic Synthesis of Chiral Building Blocks from Prochiral Substrates: Enantioselective Synthesis of Monoalkyl Malonates

✍ Prof. Dr. Manfred Schneider; Dr. Norbert Engel; Heike Boensmann 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 1 views

Enzymatic hydrolysis of prochiral cis-1,

Enzymatic hydrolysis of prochiral cis-1,4-diacyl-2-cyc-lopentenediols: preparation of (1S,4R)-and (1R,4S)-4-hydroxy-2-cyclopentenylderivatives, versatile building blocks for cyclopentanoid natural products.

✍ Kurt Laumen; Manfred Schneider 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 305 KB