Results 161 to 170 of about 18,326 (225)

Correction: Iodine-mediated synthesis of indolyl-1,3,4-thiadiazole amine derivatives and their DFT analysis. [PDF]

RSC Adv
Vaishya V, Mehra MK, Pandey SK, Pilania M.   +3 more
europepmc   +1 more source

=Evaluation of anticonvulsant effect of four new derivatives of 3 - isatinyl -2- [ 1,3,4 ] - thiadiazolyl thiosemicarbazones in the animal models of chemical PTZ seizure [PDF]

, 2015
Zafarolahi, Ali
core  

Design and Synthesis of Thiadiazole Derivatives as Dual EGFR/COX‑2 Inhibitors with Anticancer and Anti-inflammatory Activities. [PDF]

ACS Omega
Hidir A, Osmaniye D, Sağlik Özkan BN, Levent S, Kaplancikli ZA, Özkay Y.   +5 more
europepmc   +1 more source

Synthesis of 1,2,4-Triazole-3-Thiol Derivatives from Thiosemicarbazides and Carboxylic Acids Using Polyphosphate Ester. [PDF]

Molecules
Tretyakov BA, Tikhonova VI, Gadomsky SY, Sanina NA.   +3 more
europepmc   +1 more source

Synthesis of Novel Thiazole/Thiadiazole Conjugates of Fluoroquinolones as Potent Antibacterial and Antimycobacterial Agents. [PDF]

Chem Biol Drug Des
Poyraz Yılmaz P, Kulabaş N, Bozdeveci A, Vagolu SK, Imran M, Tatar E, Alpay Karaoğlu Ş, Sriram D, Mahmood AAR, Küçükgüzel İ.   +9 more
europepmc   +1 more source

Triplet states enable efficient photocatalytic hydrogen evolution in star-shaped truxene-based nanoparticles. [PDF]

Chem Sci
Brnovic A, Kumar G, Axelsson M, Cai B, Pavliuk MV, Kloo L, Hammarström L, Tian H.   +7 more
europepmc   +1 more source

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A 1,2,3-thiadiazole–1,2,3-thiadiazole rearrangement

J. Chem. Soc., Chem. Commun., 1983
During its preparation, 4-ethoxycarbonyl-5-diazomethyl-1,2,3-thiadiazole (4), undergoes a ring transformation into the isomeric structure (5), but when the ester function in (4) is replaced by a phenyl group, no isomerization is observed.
Gerrit L'abbé, Jean-Paul Dekerk, Martine Deketele   +2 more
openaire   +1 more source

The 1,2,5-Thiadiazoles

1968
Publisher Summary This chapter presents the review of organic and physical chemistry of monocyclic 1, 2, 5-thiadiazoles up to the early part of 1967. Reference is made to the 2, 1, 3-benzothiadiazoles and related compounds only as they contribute to the chemistry of the basic ring system. The 1, 2, 5-thiadiazole nucleus is numbered as in 4.
L M, Weinstock, P I, Pollak
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Microwave spectra of 1,3,4-thiadiazole and [34S]1,3,4-thiadiazole. Dipole moment of 1,3,4-thiadiazole

Journal of Molecular Spectroscopy, 1962
Abstract The microwave spectra of 1, 3, 4-thiadiazole (I) and [ 34 S] 1, 3, 4-thiadiazole (II) have been recorded in the 15,000–30,000 Mc/sec region. Twelve and ten transitions, respectively, were assigned. The rotational constants of (I) are, A = 8907.51 ± 0.10, B = 5569.27 ± 0.02, and C = 3424.80 ± 0.03 Mc/sec. For (II), A = 8908.15 ± 0.20,
Børge Bak, Daniel Christensen, Lise Hansen-Nygaard, Leif Lipschitz, John Rastrup-Andersen   +4 more
openaire   +1 more source