✦ LIBER ✦

Isomerization Polymerization of 1,3-Oxazine. I. Polymerization of Unsubstituted 5,6-Dihydro-4H-1,3-oxazine Giving Poly(N-formyltrimethylenimine) and Its Alkaline Hydrolysis of Poly(trimethylenimine)

✍ Scribed by Saegusa, Takeo; Nagura, Yoshitomi; Kobayashi, Shiro

Book ID: 123618072
Publisher: American Chemical Society
Year: 1973
Tongue: English
Weight: 462 KB
Volume: 6
Category: Article
ISSN: 0024-9297
DOI: 10.1021/ma60034a004

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Isomerization Polymerization of 1,3-Oxaz

Isomerization Polymerization of 1,3-Oxazine. II. Kinetic Studies of the Ring-Opening Isomerization Polymerization of Unsubstituted 5,6-Dihydro-4H-1,3,-oxazine

✍ Saegusa, Takeo; Kobayashi, Shiro; Nagura, Yoshitomi 📂 Article 📅 1974 🏛 American Chemical Society 🌐 English ⚖ 818 KB

Ring-opening polymerization of 5,6-dihyd

Ring-opening polymerization of 5,6-dihydro-4H-1,3-oxazin-6-ones, six-membered "azlactones", to poly(N-acyl-β-peptides)

✍ Kobayashi, Shiro; Tsukamoto, Yoshihisa; Saegusa, Takeo 📂 Article 📅 1990 🏛 American Chemical Society 🌐 English ⚖ 484 KB

Isomerization Polymerization of 1,3-Oxaz

Isomerization Polymerization of 1,3-Oxazine. III. Kinetic Studies in the Ring-Opening Polymerization of 2-Phenyl-5,6-dihydro-4H-1,3-oxazine by Methyl Tosylate and Methyl Iodide Initiators

✍ Saegusa, Takeo; Kobayashi, Shiro; Nagura, Yoshitomi 📂 Article 📅 1974 🏛 American Chemical Society 🌐 English ⚖ 618 KB

Chemistry of isocyanic acid and its deri

Chemistry of isocyanic acid and its derivatives. I. Preparation, polymerization, and decomposition of 3,4,5,6-tetrahydro-2,4-dioxo-2H-1,3-oxazines

✍ Ozaki, Shoichiro ;Kato, Takazo 📂 Article 📅 2007 🏛 Wiley (John Wiley & Sons) ⚖ 375 KB

Microwave Accelerated Polymerization of

Microwave Accelerated Polymerization of 2-Phenyl-5,6-dihydro-4H-1,3-oxazine: Kinetics and Influence of End-Groups on Glass Transition Temperature

✍ Sebastian Sinnwell; Helmut Ritter 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 147 KB

## Abstract **Summary:** The ring‐opening polymerizations of 2‐phenyl‐5,6‐dihydro‐4__H__‐1,3‐oxazine (PhOZI) with methyl tosylate (MeOTs) and butyl iodide (BuI) as initiators were performed in refluxing butyronitrile. Reaction kinetics under microwave irradiation was compared with conventional oil

ChemInform Abstract: Cycloaddition/Ring

ChemInform Abstract: Cycloaddition/Ring Opening of 3-Unsubstituted Cyclic Nitronates, Isoxazoline and 5,6-Dihydro-4H-1,2-oxazine N-Oxides, as Synthetic Equivalents of Functionalized Nitrile Oxides.

✍ S. KANEMASA; T. YOSHIMIYA; E. WADA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Cycloaddition/Ring Opening of 3-Unsubstituted Cyclic Nitronates, Isoxazoline and 5,6-Dihydro-4H-1,2-oxazine N-Oxides, as Synthetic Equivalents of Functionalized Nitrile Oxides. -Treatment of 3-halo-1-nitropropane [cf. (I)] with base results in cyclization to a nitronate. Trapping with electron-rich