✦ LIBER ✦

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

✍ Scribed by Kobayashi, Shiro; Tsukamoto, Yoshihisa; Saegusa, Takeo

Book ID: 125461264
Publisher: American Chemical Society
Year: 1990
Tongue: English
Weight: 484 KB
Volume: 23
Category: Article
ISSN: 0024-9297
DOI: 10.1021/ma00212a002

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

Isomerization Polymerization of 1,3-Oxaz

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)

✍ Saegusa, Takeo; Nagura, Yoshitomi; Kobayashi, Shiro 📂 Article 📅 1973 🏛 American Chemical Society 🌐 English ⚖ 462 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

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

N-Thioacyl 1,3-Amino Alcohols: Synthesis

N-Thioacyl 1,3-Amino Alcohols: Synthesis via Ring-Opening of Oxiranes with Thioamide Dianions and Applications as Key Intermediates Leading to Stereochemically Defined 5,6-Dihydro-4H-1,3-oxazines and 1,3-Amino Alcohols.

✍ Toshiaki Murai; Hiroaki Sano; Hiroyasu Kawai; Hideo Aso; Fumitoshi Shibahara 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 48 KB

N -Thioacyl 1,3-Amino Alcohols: Synthesi

N -Thioacyl 1,3-Amino Alcohols: Synthesis via Ring-Opening of Oxiranes with Thioamide Dianions and Applications as Key Intermediates Leading to Stereochemically Defined 5,6-Dihydro-4 H -1,3-oxazines and 1,3-Amino Alcohols

✍ Murai, Toshiaki; Sano, Hiroaki; Kawai, Hiroyasu; Aso, Hideo; Shibahara, Fumitosh 📂 Article 📅 2005 🏛 American Chemical Society 🌐 English ⚖ 154 KB