91109-12-5Relevant academic research and scientific papers
BENZENESULFONYLCARBONITRILE OXIDE. 5. FACE SELECTIVITY OF CYCLOADDITION TO CHIRAL TERMINAL ALKENES
Wade, Peter A.,Singh, Shankar M.,Pillay, M. Krishna
, p. 601 - 612 (2007/10/02)
The diastereomer ratio for cycloaddition of benzenesulfonylcarbonitrile oxide (BSNO) to a series of (S)-vinylglycine-derived alkenes varied from 30:70 to 66:34 depending on the substituents at the chiral center.Isomer ratios were routinely determined by (
FUROXANS AS NITRILE OXIDE PRECURSORS: CYCLOADDITION REACTIONS OF BIS(BENZENESULFONYL)FUROXAN.
Whitney, Ralph A.,Nicholas, Everton S.
, p. 3371 - 3374 (2007/10/02)
Bis(benzenesulfonyl)furoxan has been shown to undergo cycloaddition reactions with dipolarophiles in refluxing xylene to give benzenesulfonylnitrile oxide cycloadducts.
