Intermolecular annulation of enynes and propargyl esters to selectively produce styrenes or fluorenes is reported. The divergent arene syntheses involve a Au-catalyzed, two-pot, multistep process proceeding by cis-diastereoselective cyclopropanation, cycloisomerization, and, finally, annulation or elimination.

Abstract Direct D-H exchange in radicals is investigated a quasi-uniform flow employing chirped-pulse millimeter-wave spectroscopy. Inspired by the H-atom catalyzed isomerization of C 3 H 2 reported our previous study, D-atom reactions with propargyl (C ) radical and its photoproducts were investigated. We observed very efficient enrichment through an analogous process D addition/H elimination ...

Gold-catalyzed synthesis of buta-1,3-dien-2-yl esters by the reaction of propargyl esters with vinylazides is described; the reaction mechanism is postulated to involve a vinyl attack of vinylazides at alkenyl gold carbenes.

The electrochemical intramolecular cyclization of propargyl derivatives containing a carbon–halogen bond in N,N’-dimethylformamide at constant current in a diaphragmless cell has been developed using Ni(II) complexes as electron-transfer mediators.

in order to examination of dual purpose herbicides on some wheat physiological indexes in different stages of phenology of this corp, an experiment was conducted in 1386-1387, in kordkoy, golestan province with dry farming condition. this study was performed as factorial in randomized complete block design with 2 factors and 4 replications. the first factor included the type of herbicides: shov...

Substituted naphthofurans and naphthopyrans were constructed at high temperature from allyl or propargyl naphthyl ethers via Claisen rearrangement in moderate to good yields. Also, substituted (trimethylsilyl)-naphthofurans were synthesized from the corresponding naphtofurans.

Duplex DNA with terminal and internal sugar cross-links were synthesized by the CuAAC reaction from oligonucleotides containing 2'-O-propargyl-2-aminoadenosine as a clickable site and a bifunctional azide (4). Stepwise click chemistry was employed to introduce cross-links at internal and terminal positions. Copper turnings were used as catalyst, reducing the copper load of the reaction mixture ...

Synthesis and biological evaluation are described of seven new analogues (3-9) of two potent thymidylate synthase inhibitors, 10-propargyl-5,8-dideazafolate (1) and its 2-methyl-2-deamino congener ICI 198583 (2). While the new compunds 3 and 4 were analogues of 1 and 2, respectively, containing a p-aminobenzenesulfonyl residue in place of the p-aminobenzoic acid residue, the remaining 5 new com...