✦ LIBER ✦

Carbodiimides. I. Conversion of Isocyanates to Carbodiimides with Phospholine Oxide Catalyst

✍ Scribed by Campbell, Tod W.; Monagle, John J.; Foldi, Veronika S.

Book ID: 111986570
Publisher: American Chemical Society
Year: 1962
Tongue: English
Weight: 681 KB
Volume: 84
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00878a015

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Carbodiimides. III. Conversion of Isocya

Carbodiimides. III. Conversion of Isocyanates to Carbodiimides. Catalyst Studies

✍ Monagle, John J. 📂 Article 📅 1962 🏛 American Chemical Society 🌐 English ⚖ 593 KB

New Catalysts for the Conversion of Isoc

New Catalysts for the Conversion of Isocyanates to Carbodiimides

✍ Dyer, Elizabeth; Read, Robert E. 📂 Article 📅 1961 🏛 American Chemical Society 🌐 English ⚖ 249 KB

Metal carbonyls as catalysts in the conv

Metal carbonyls as catalysts in the conversion of isocyanates to carbodiimides

✍ Henri Ulrich; B. Tucker; A.A.R. Sayigh 📂 Article 📅 1967 🏛 Elsevier Science 🌐 French ⚖ 146 KB

Additions and Corrections: New Catalysts

Additions and Corrections: New Catalysts for the Conversion of Isocyanates to Carbodiimides

✍ Dyer, Elizabeth; Read, Robert 📂 Article 📅 1962 🏛 American Chemical Society 🌐 English ⚖ 125 KB

Catalytic Conversion of Isocyanates to C

Catalytic Conversion of Isocyanates to Carbodiimides by Cyclopentadienyl Manganese Tricarbonyl and Cyclopentadienyl Iron Dicarbonyl Dimer.

✍ A. K. Fazlur Rahman; Kenneth M. Nicholas 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 18 KB

Cycloaddition of Carbodiimides with a He

Cycloaddition of Carbodiimides with a Heteroaromatic Substituent to Allenic Acids

✍ Latchezar S. Trifonov; Nadja I. Christova; Valentin S. Dimitrov; Alexander S. Or 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 German ⚖ 227 KB 👁 1 views

Cycloaddition of the allenic acid 3 with the N-cyclohexyl-N'-heteroaromatic carbodiimides 2a and 2b gave the isomeric pyrido[l,2-~]pyrimidinones 4 and 5 and thiazolo[3,2-~]pyrimidinones 6 and 7, respectively, instead of the expected Diels-Alder adducts analogous to 1. The compounds of the latter typ