𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and oxidation of chiral 2-thiazolines (4,5-dihydro-1,3-thiazoles)

✍ Scribed by Aitken, R. Alan; Armstrong, David P.; Galt, Ronald H. B.; Mesher, Shaun T. E.

Book ID
111949860
Publisher
Royal Society of Chemistry
Year
1997
Weight
537 KB
Volume
6
Category
Article
ISSN
1472-7781

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis and Oxida
ChemInform Abstract: Synthesis and Oxidation of Chiral 2-Thiazolines (4,5-Dihydro-1,3- thiazoles).
✍ R. A. AITKEN; D. P. ARMSTRONG; R. H. B. GALT; S. T. E. MESHER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Synthesis and Oxidation of Chiral 2-Thiazolines (4,5-Dihydro-1,3thiazoles). -Eight new chiral thiazolines (IV) and (X) are prepared by treatment of oxazolines (III) or alcohols (IX) with P2S5. These thiazolines are oxidized using various agents. -(AITKEN, R. A.; ARMSTRONG, D. P.;

Synthesis, structure, and oxidation of 3
Synthesis, structure, and oxidation of 3,4-dihydro-1,2,5-benzotrithiepins
✍ Satoshi Ogawa; Masaki Sasaki; Takayuki Ogasawara; Ryu Sato; Yasushi Kawai 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 695 KB

## Abstract Stable benzene‐fused polysulfide compounds, 3,4‐dihydro‐1,2,5‐benzotrithiepins (1a‐c), have been prepared, and the structure of 1a has been determined by X‐ray crystallographic analysis. While the electrophilic oxidation of compounds 1 with m‐chloroperbenzoic acid gave the corresponding

Efficient synthesis of 5-(2-hydroxyethyl
Efficient synthesis of 5-(2-hydroxyethyl)-2-phenylimino- 1,3-thiazolidin-4-ones and 5-(2-hydroxyethyl)-2-phenylamino-4,5-dihydro-1,3-thiazol-4-ones
✍ Jiří Váňa; Jiří Hanusek; Aleš Růžička; Miloš Sedlák 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 159 KB 👁 1 views

## Abstract magnified image A new method for the synthesis of substituted 5‐(2‐hydroxyethyl)‐2‐phenylimino‐1,3‐thiazolidin‐4‐ones and 5‐(2‐hydroxyethyl)‐2‐phenylamino‐4,5‐dihydro‐1,3‐thiazol‐4‐ones is described, starting from phenylthioureas and 3‐bromotetrahydrofuran‐2‐one. The reaction proceeds