Results 171 to 180 of about 13,350 (226)

Sustainable Joullié-Ugi and Continuous Flow Implementation Led to Novel Captopril-Inspired Broad-Spectrum Metallo-β-Lactamase Inhibitors. [PDF]

J Med Chem
Alfano AI, Pelliccia S, Barone S, Cutarella L, Cancade SMI, Baia V, Cassese E, Russomanno P, Messano N, Frank D, Weizel L, Rotter MJ, Brunst S, Wichelhaus TA, Proschak E, Tedesco D, Mori M, Docquier JD, Summa V, Brindisi M.   +19 more
europepmc   +1 more source

Correction: Wu et al. Synthesis of Spirooxindole-O-Naphthoquinone-Tetrazolo[1,5-a]Pyrimidine Hybrids as Potential Anticancer Agents. Molecules 2018, 23, 2330. [PDF]

Molecules
Wu L, Liu Y, Li Y.
europepmc   +1 more source

The Substrate Versatility of Δ¹-Pyrroline-5-carboxylate Reductase (ProC) from <i>Escherichia coli</i>. [PDF]

Molecules
Polverini E, Vecchi A, Capra G, Pastori A, Peracchi A.   +4 more
europepmc   +1 more source

New spirooxindole pyrrolidine/pyrrolizidine analogs: design, synthesis, and evaluation as an anticancer agent. [PDF]

RSC Adv
Nivetha N, Venkatesan J, Murugan D, Rangasamy L, Wu SP, Velmathi S.   +5 more
europepmc   +1 more source

Total Synthesis of (-)-Owerreine and (-)-Anhydrovobtusine. [PDF]

Org Lett
Myeong IS, Pinto T, Movassaghi M.
europepmc   +1 more source

Synthesis, Biological Evaluation, and Molecular Docking Studies of Novel Coumarin-Triazole-Isatin Hybrids as Selective Butyrylcholinesterase Inhibitors. [PDF]

Molecules
Dimkovski A, Dobričić V, Simić MR, Jurhar Pavlova M, Mihajloska E, Sterjev Z, Poceva Panovska A.   +6 more
europepmc   +1 more source

Pathway economy in cyclization of 1<i>,n</i>-enynes. [PDF]

Beilstein J Org Chem
Han H, Mao W, Lin B, Cheng M, Yang L, Liu Y.   +5 more
europepmc   +1 more source

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Diastereoselective synthesis of functionalized spiro[cyclopropane-1,3′-indolines] and spiro[indoline-3,1′-cyclopropane-2′,3″-indolines]

Tetrahedron, 2016
In the presence of hexamethylphosphorous triamide, the reaction of isatin with arylidene pivaloylacetonitriles in dry methylene dichloride afforded functionalized spiro[cyclopropane-1,3′-indolines] in good yields and with high diastereoselectivity.
Chao-Guo Yan
exaly   +3 more sources

N-(Cyanothioformyl)indoline; a new indoline ring forming reaction

Journal of the Chemical Society, Perkin Transactions 1, 1998
Conversion of 2-hydroxymethyl- and 2-hydroxyethylaniline with Appel salt 1 into the arylimines 3 and 4 is accompanied by formation of the chloromethyl and chloroethyl derivatives 8 and 9. Triphenylphosphine converts compound 8 into the benzothiazine 6 but the chloroethyl compound 9 gives N-(cyanothioformyl)indoline 10 (55%) rather than the analogous ...
Besson, Thierry, Guillaumet, Gerald, Lamazzi, Christelle, Rees, Charles, Thiéry, Valérie   +4 more
openaire   +2 more sources

Photolysis of indoline

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1986
The quantum yields of photodissociation and fluorescence of a solution of indoline in heptane were determined for various wavelengths. The quantum yield of photodissociation increases with increasing excitation energy.
Sh. Ruziev, A. S. Dvornikov, Ya. N. Malkin, V. A. Kuz'min   +3 more
openaire   +1 more source