340258-57-3Relevant articles and documents
Direct transformation of arylpropynes to acrylamides via a three-step tandem reaction
Qiu, Jun,Zhang, Ronghua
supporting information, p. 1556 - 1560 (2014/03/21)
A novel and metal-free acrylamides formation between arylpropynes and hydroxylamine hydrochloride through sp3 C-H and C-C bond cleavage has been achieved with DDQ as an oxidant. The mechanistic study shows that the acrylamides are formed through a three-step tandem sequence, including cross-dehydrogenative-coupling (CDC) reaction, aza-Meyer-Schuster rearrangement and Beckmann rearrangement. This journal is The Royal Society of Chemistry 2014.
Stereoselective synthesis of (2E)-cinnamanilides via desulfonylation of (2E)-α-amino-α,β-unsaturated sulfones by samarium/glacial acetic acid/ethanol system
Liu, Yunkui,Zhang, Yongmin
, p. 372 - 375 (2007/10/03)
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