✦ LIBER ✦

Synthesis and reactions of Biginelli-compounds. Part 14.1 A rhodium-induced cyclization–cycloaddition sequence for the construction of conformationally rigid calcium channel modulators of the dihydropyrimidine type

✍ Scribed by Jauk, Birgit; Belaj, Ferdinand; Kappe, C. Oliver

Book ID: 120296459
Publisher: Royal Society of Chemistry
Year: 1999
Weight: 289 KB
Volume: 3
Category: Article
ISSN: 1472-7781
DOI: 10.1039/A808594C

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis and React

ChemInform Abstract: Synthesis and Reactions of Biginelli-Compounds. Part 14. A Rhodium-Induced Cyclization—Cycloaddition Sequence for the Construction of Conformationally Rigid Calcium Channel Modulators of the Dihydropyrimidine Type.

✍ Birgit Jauk; Ferdinand Belaj; C. Oliver Kappe 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

ChemInform Abstract: Synthesis and React

ChemInform Abstract: Synthesis and Reactions of Biginelli Compounds. Part 10. Synthesis and Aromatization of Dihydropyrimidines Structurally Related to Calcium Channel Modulators of the Nifedipine-Type.

✍ J. J. VANDEN EYNDE; N. AUDIART; V. CANONNE; S. MICHEL; Y. VAN HAVERBEKE; C. O. K 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis and Reactions of Biginelli Compounds. Part 10. Synthesis and Aromatization of Dihydropyrimidines Structurally Related to Calcium Channel Modulators of the Nifedipine-Type. -By employing the "Hideg-modification" of the Biginelli reaction a number of 1,4-dihydropyrimidines (IV) (8 examples)