✦ LIBER ✦

ChemInform Abstract: Methodologies for the Stereoselective Synthesis of Adrenergic β-Blockers: an Overview.

✍ Scribed by C. Campo; E. F. Llama; J. L. Bermudez; J. V. Sinisterra

Publisher: John Wiley and Sons
Year: 2010
Weight: 27 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200203265

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Main Methodologies

ChemInform Abstract: Main Methodologies for the Synthesis of Radialenes. An Update

✍ Florence Geneste; Alec Moradpour 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB

ChemInform Abstract: A New Methodology f

ChemInform Abstract: A New Methodology for the Synthesis of β-Amino Acids.

✍ Mukund P. Sibi; Prasad K. Deshpande 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Highly Stereoselective Reduction of Halo

Highly Stereoselective Reduction of Haloketones Using Three New Yeasts: Application to the Synthesis of (S)-Adrenergic β-Blockers Related to Propranolol.

✍ Fernando Martinez Lagos; Jose D. Carballeira; Jose L. Bermudez; Emilio Alvarez; 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 141 KB

ChemInform Abstract: Convenient Methodol

ChemInform Abstract: Convenient Methodology for the Synthesis of Trialkylhydrazines.

✍ Alvaro J. Vazquez; Cristian Rodriguez; N. Sbarbati Nudelman 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

ChemInform Abstract: New Methodologies f

ChemInform Abstract: New Methodologies for the Synthesis of Compound Libraries

✍ Shu Kobayashi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

ChemInform Abstract: Novel Methodologies

ChemInform Abstract: Novel Methodologies for the Synthesis of Functionalized Pyroglutamates.

✍ Srinivas Tekkam; M. A. Alam; Subash C. Jonnalagadda; Venkatram R. Mereddy 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

## Abstract A series of pyroglutamates (III), (VIII), and (X) is readily prepared by reaction of iminoesters (I) with corresponding Baylis—Hillman derivatives followed by acidic cleavage of imines and a subsequent lactamization.