✦ LIBER ✦

2-Aminoarylation of heterocycles via a benzidine-like rearrangement

✍ Scribed by Sheradsky, Tuvia; Nov, Eliahu; Avramovici-Grisaru, Schely

Book ID: 120933780
Publisher: Royal Society of Chemistry
Year: 1979
Weight: 408 KB
Category: Article
ISSN: 1472-7781
DOI: 10.1039/P19790002902

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel rearrangement of 1-(2-aminoaryl)

A novel rearrangement of 1-(2-aminoaryl)imidazoles

✍ John W. Lampe; Susan V. Di Meo; Joseph A. Traina 📂 Article 📅 1994 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 413 KB

Synthesis of a biphenyl-based cyclophane

Synthesis of a biphenyl-based cyclophane via benzidine rearrangement of a constrained m-nitrophenol derivative

✍ Andrew C. Benniston; William Clegg; Anthony Harriman; Ross W. Harrington; Peiyi 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 198 KB

The benzidine rearrangement of a constrained m-nitrophenol derivative results in production of a cyclophane comprising a biphenyl group and a polyether tether connected at the 4,4% positions.

Hydrolytic cleavages of 7-nitro-2-phenyl

Hydrolytic cleavages of 7-nitro-2-phenyl-1,2-benzisoxazol-3-one. Evidence for the occurrence of a benzidine-like rearrangement of N,O-diphenylhydroxylamines

✍ Tuvia Sheradsky; Schely Avramovici-Grisaru 📂 Article 📅 1980 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 106 KB

Synthesis via sigmatropic rearrangement.

Synthesis via sigmatropic rearrangement. 2. Regiospecific synthesis of 2,3-disubstituted furans, pyrroles, and thiophenes. Claisen ortho ester rearrangement of heterocyclic glycolates

✍ Raucher, Stanley; Lui, Alfred S. T.; Macdonald, James E. 📂 Article 📅 1979 🏛 American Chemical Society 🌐 English ⚖ 434 KB

Notes- Synthesis of 2-Chlorophenonthiazi

Notes- Synthesis of 2-Chlorophenonthiazine via a Smiles Rearrangement

✍ Galbreath, Robert; Ingham, Robert 📂 Article 📅 1958 🏛 American Chemical Society 🌐 English ⚖ 415 KB

A total synthesis of magallanesine via [

A total synthesis of magallanesine via [1, 2]-Meisenheimer rearrangement

✍ Ryuji Yoneda; Yasuhiko Sakamoto; Yoshifumi Oketo; Kayoko Minami; Shinya Harusawa 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 257 KB

A straightforward synthesis of magallanesine 1 from azetoisoquinoline 4 has been accomplished via [ 1.21~Meisenheimer rearrangement and an intramolecular Heck cyclization as the key reactions. Members of the plant family Berberidaceae have long been known to contain a number of alkaloids, and recent