69489-56-1Relevant academic research and scientific papers
Microwave mediated synthesis of spiro-(indoline-isoxazolidines): Mechanistic study and biological activity evaluation
Raunak,Kumar, Vineet,Mukherjee, Shubhasish,Poonam,Prasad, Ashok K.,Olsen, Carl E.,Sch?ffer, Susan J.C.,Sharma, Sunil K.,Watterson, Arthur C.,Errington, William,Parmar, Virinder S.
, p. 5687 - 5697 (2005)
Regioisomeric spiro-(indoline-isoxazolidines) have been synthesized in moderate yields by the cycloaddition reaction between ethyl (3-indolylidene) acetate and various substituted α,N-diphenylnitrones, using environmentally benign microwave technology. A
Synthetic and biological activity evaluation studies on novel isoxazolidines
Mukherjee, Shubhasish,Raunak,Dhawan, Ashish,Poonam,Prasad, Ashok K.,Olsen, Carl E.,Cholli, Ashok L.,Errington, William,Raj, Hanumantharao G.,Watterson, Arthur C.,Parmar, Virinder S.
, p. 2670 - 2682 (2007/10/03)
Enantioselective deacetylation reactions on 5-acetoxymethyl- and 5-acetoxy-3-aryl-2-phenylisoxazolidines using Candida rugosa lipase (CRL) are described. Varying degrees of enantioselectivity have been observed depending on the nature of the 3-aryl group.
