Synthesis and Beckmann rearrangement of novel (Z)-2-organylselanyl ketoximes: promising agents against grapevine anthracnose infection

Comprehensive updates on Beckmann Rearrangement

“…Beckmann rearrangement of selanyl ketoxime to N‐aryl‐2‐(selanyl)acetamides 77 achieved in excellent yield [120] . (Scheme 86).…”

Crystal structure of bis(acetato-κ1 O)-bis(1-(pyridin-2-yl)ethan-1-one oxime-κ2 N,N′)zinc(II), C18H22N4O6Zn

“…Pyridyl oximes have the general formula (py)C(R)NOH, where py is a pyridyl group attached to the oxime carbon atom and R can be a donor or a non-donor group [4]. Pyridyl oximes ligands represent one of the most widely utilized classes of ligands in coordination chemistry [5].…”

Organoselenium Chemistry

“…[15][16][17][18] More commonly, synthetic transformations such as selenenylations, selenocyclizations and 2,3-sigmatropic rearrangements have been successfully achieved using these reagents under mild reaction conditions. [19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] The application of these reagents in catalysis makes them more suitable reagents in organic synthesis. [34][35][36][37][38][39] Several books, [1][2][3][4][5][6][7][41][42][43] book chapters [8][9][10][11][44][45][46][47][48] and review articles [49][50][51][52][53]…”