1219938-39-2Relevant academic research and scientific papers
An improved synthesis of 1,2-benzisoxazoles: TBAF mediated 1,3-dipolar cycloaddition of nitrile oxides and benzyne
Spiteri, Christian,Sharma, Pallavi,Zhang, Fengzhi,MacDonald, Simon J. F.,Keeling, Steve,Moses, John E.
supporting information; experimental part, p. 1272 - 1274 (2010/07/05)
An efficient synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reaction partners medi
An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne
Spiteri, Christian,Mason, Christopher,Zhang, Fengzhi,Ritson, Dougal J.,Sharma, Pallavi,Keeling, Steve,Moses, John E.
experimental part, p. 2537 - 2542 (2010/07/16)
An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reactants simultaneously. The Royal Society of Chemistry 2010.
