Works matching IS 07930283 AND DT 2016 AND VI 22 AND IP 6
Results: 10
Pyrimidinethione as a building block in heterocyclic synthesis: synthesis of pyrano[2,3- d]pyrimidine, chromeno[2,3- d]pyrimidine, pyrido[3′,2′:5,6]pyrano[2,3- b]pyridine, and pyrimido[5′,4′:5,6]pyrano[2,3- d]pyrimidine derivatives
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 311, doi. 10.1515/hc-2016-0039
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C<sup>1</sup>-Substituted N- tert-butoxycarbonyl-5- syn- tert-butyldimethylsilyloxymethyl-2-azabicyclo[2.1.1]hexanes as conformationally constrained β-amino acid precursors.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 319, doi. 10.1515/hc-2016-0046
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Synthesis and biological evaluation of 4-(2′,4′-difluorobiphenyl-4-yl)-6-arylpyrimidin- 2-amine derivatives.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 351, doi. 10.1515/hc-2016-0050
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Synthesis and characterization of 1,3,4-thiadiazole-2,5-dithio crown ethers.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 329, doi. 10.1515/hc-2016-0097
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Oxidative reaction of 2-aminopyridine-3-sulfonyl chlorides with tertiary amines.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 333, doi. 10.1515/hc-2016-0102
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Synthesis and antimicrobial properties of cycloheptyl substituted benzimidazolium salts and their silver(I) carbene complexes.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 357, doi. 10.1515/hc-2016-0105
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Solvent-free microwave-assisted synthesis and biological evaluation of 2,2-dimethylchroman-4-one based benzofurans.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 363, doi. 10.1515/hc-2016-0147
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- Article
New 8-substituted BODIPY-based chromophores: synthesis, optical and electrochemical properties.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 339, doi. 10.1515/hc-2016-0151
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Heterocyclization of 5,6-disubstituted 3-alkenyl-2-thioxothieno[2,3- d]pyrimidin-4-one with p-alkoxyphenyltellurium trichloride.
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- Heterocyclic Communications, 2016, v. 22, n. 6, p. 347, doi. 10.1515/hc-2016-0169
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Frontmatter.
- Published in:
- Heterocyclic Communications, 2016, v. 22, n. 6, p. i, doi. 10.1515/hc-2016-frontmatter1
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- Article