96159-92-1Relevant academic research and scientific papers
A single-reagent-driven multistep one-pot preparation of thiazolines and 1,3-thiazines from aldoximes, nitriles, and carboxylic acids
Bhattacharyya, Shubhankar,Pathak, Uma
, p. 3553 - 3560 (2015/11/17)
N-(ω-Bromoalkyl)dichlorothiophosphoramidates have been designed as a new class of reagent for the single-reagent-driven multistep preparation of 2-substituted thiazolines and 1,3-thiazines from ald-oximes, nitriles, or carboxylic acids. A wide range of substrates both aromatic as well as aliphatic were investigated and found suitable for the developed protocol.
Synthesis of thiazolines by the reaction of aryl ketonitriles with cysteamine via microwave irradiation
Kamila, Sukanta,Biehl, Edward R.
, p. 407 - 409 (2008/03/29)
(Chemical Equation Presented) Thiazolines were synthesized in a one-pot reaction in excellent yield using a newly developed methodology. Ketonitriles were directly condensed with cysteamine (2-amino-thioalcohol) via microwave irradiation at 210°C for 10 m
Research on radioprotective agents: Δ-2 Thiazolines and homologous derivatives
Robbe,Fernandez,Chapat,et al.
, p. 16 - 24 (2007/10/02)
Compounds derived from Δ-2 thiazoline, Δ-2 thiazolinium iodoalkylate and 4,5-dihydro-1,3 thiazine have been prepared and evaluated as potential antiradiation agents in mice. They generally have a low toxicity and significant radioprotective activity.
