Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1967, 32, 2155-2160
https://doi.org/10.1135/cccc19672155

Synthetic reactions of dimethylformamide. XXIII. Formylation of some aliphatic diazo compounds

F. M. Stojanovič and Z. Arnold

Crossref Cited-by Linking

  • Zhang Jiantao, Xu Jiaxi: Chemoselectivity in the Reaction of 2‐Diazo‐3‐oxo‐3‐phenylpropanal with Aldehydes and Ketones. Helvetica Chimica Acta 2013, 96, 1733. <https://doi.org/10.1002/hlca.201200532>
  • Wang Zikun, Bi Xihe, Liao Peiqiu, Zhang Rui, Liang Yongjiu, Dong Dewen: Intramolecular hydrogen bonding-assisted cyclocondensation of α-diazoketones with various amines: a strategy for highly efficient Wolff 1,2,3-triazole synthesis. Chem. Commun. 2012, 48, 7076. <https://doi.org/10.1039/c2cc33157h>
  • Qi Hengzhen, Li Xinyao, Xu Jiaxi: Stereoselective control in the Staudinger reactions involving monosubstituted ketenes with electron acceptor substituents: experimental investigation and theoretical rationalization. Org. Biomol. Chem. 2011, 9, 2702. <https://doi.org/10.1039/c0ob00783h>
  • Ferreira Sabrina B., Costa Marilia S., Boechat Núbia, Bezerra Rômulo J.S., Genestra Marcelo S., Canto-Cavalheiro Marilene M., Kover Warner B., Ferreira Vitor F.: Synthesis and evaluation of new difluoromethyl azoles as antileishmanial agents. European Journal of Medicinal Chemistry 2007, 42, 1388. <https://doi.org/10.1016/j.ejmech.2007.02.020>
  • Costa Marilia S., Boechat Núbia, Rangel Érica A., da Silva Fernando de C., de Souza Alessandra M.T., Rodrigues Carlos R., Castro Helena C., Junior Ivan N., Lourenço Maria Cristina S., Wardell Solange M.S.V., Ferreira Vitor F.: Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives. Bioorganic & Medicinal Chemistry 2006, 14, 8644. <https://doi.org/10.1016/j.bmc.2006.08.019>
  • Dabak Kadir, Sezer Özkan, Akar Ahmet, Anaç Olcay: Synthesis and investigation of tuberculosis inhibition activities of some 1,2,3-triazole derivatives. European Journal of Medicinal Chemistry 2003, 38, 215. <https://doi.org/10.1016/S0223-5234(02)01445-9>
  • Dabak Kadir, Akar Ahmet: SYNTHESIS OF 1-VINYL 1,2,3-TRIAZOLE DERIVATIVES. Heterocyclic Communications 2002, 8. <https://doi.org/10.1515/HC.2002.8.1.61>
  • Dabak Kadir, Akar Ahmet: SYNTHESIS OF 1,2,3-TRIAZOLE DERIVED POTENTIAL PEPTIDOMIMETICS. Heterocyclic Communications 2002, 8. <https://doi.org/10.1515/HC.2002.8.4.385>
  • Hallinan E.Ann, Hagen Timothy J., Tsymbalov Sofya, Stapelfeld Awilda, Savage Michael A.: 2,4-Disubstituted oxazoles and thiazoles as latent pharmacophores for diacylhydrazine of SC-51089, a potent PGE2 antagonist. Bioorganic & Medicinal Chemistry 2001, 9, 1. <https://doi.org/10.1016/S0968-0896(00)00229-7>
  • Jiang Lu, Davison Amanda, Tennant George, Ramage Robert: Synthesis and application of a novel coupling reagent, ethyl 1-hydroxy-1H -1,2,3-triazole-4-carboxylate. Tetrahedron 1998, 54, 14233. <https://doi.org/10.1016/S0040-4020(98)00876-X>
  • Sezer Özhan, Dabak Kadir, Anaç Olcay, Akar Ahmet: Diazoaldehyde Chemistry. Part 4vilsmeier‐haack formylation of diazo compounds: A re‐investigation. Helvetica Chimica Acta 1997, 80, 960. <https://doi.org/10.1002/hlca.19970800327>
  • Romeiro Gilberto A., Pereira Letícia O.R., de Souza Maria Cecília B.V., Ferreira Vitor F., Cunha Anna Claudia: A new and efficient procedure for preparing 1,2,3-triazoles. Tetrahedron Letters 1997, 38, 5103. <https://doi.org/10.1016/S0040-4039(97)01137-4>
  • Sezer Özkan, Dabak Kadir, Akar Ahmet, Anaç Olcay: Diazoaldehyde Chemistry. Part 3. Synthesis of 4‐acyl‐1H‐1,2,3‐triazole derivatives. Helvetica Chimica Acta 1996, 79, 449. <https://doi.org/10.1002/hlca.19960790212>
  • Sezer Özkan, Anaç Olcay: Diazoaldehyde Chemistry. Part 1. Transdiazotization of Acylacetaldehydes in Neutral‐to‐Acidic Medium. A Direct Approach to the Synthesis of α‐Diazo‐β‐oxoaldehydes. Helvetica Chimica Acta 1994, 77, 2323. <https://doi.org/10.1002/hlca.19940770819>
  • Connell Richard D., Tebbe Mark, Gangloff Anthony R., Helquist Paul, Åkermark Björn: Rhodium-catalyzed heterocycloaddition route to 1,3-oxazoles as building blocks in natural products synthesis. Tetrahedron 1993, 49, 5445. <https://doi.org/10.1016/S0040-4020(01)87261-6>
  • Clarke David, Mares Richard W., McNab Hamish: A novel entry to the imidoylketene–oxoketenimine energy surface. J. Chem. Soc., Chem. Commun. 1993, 1026. <https://doi.org/10.1039/C39930001026>
  • Franchetti P., Messini L., Cappellacci L., Grifantini M., Guarracino P., Marongiu M. E., Piras G., Colla P. La: A New Facile Synthesis and Antiviral Activity of Oxazofurin. Nucleosides and Nucleotides 1993, 12, 359. <https://doi.org/10.1080/07328319308017832>
  • Connell Richard D, Tebbe Mark, Helquist Paul, Åkermark Björn: Direct preparation of 4-carboethoxy-1,3-oxazoles. Tetrahedron Letters 1991, 32, 17. <https://doi.org/10.1016/S0040-4039(00)71206-8>
  • Bakulev V. A., Mokrushin V. S.: Structures synthesis, and properties of 1,2,3-thiadiazoles (review). Chem Heterocycl Compd 1986, 22, 811. <https://doi.org/10.1007/BF01175051>
  • Olesen Preben H., Nielsen Flemming E., Pedersen Erik B., Becher Jan: Heterocyclic studies. 2. 5‐Chloro‐1H‐1,2,3‐triazole‐4‐carboxaldehydes, preparation and rearrangement reactions. Journal of Heterocyclic Chem 1984, 21, 1603. <https://doi.org/10.1002/jhet.5570210607>
  • Meier Herbert, Zeller Klaus‐Peter: Die Wolff‐Umlagerung von α‐Diazocarbonyl‐Verbindungen. Angewandte Chemie 1975, 87, 52. <https://doi.org/10.1002/ange.19750870203>
  • Meier Herbert, Zeller Klaus‐Peter: The Wolff Rearrangement of α‐Diazo Carbonyl Compounds. Angew. Chem. Int. Ed. Engl. 1975, 14, 32. <https://doi.org/10.1002/anie.197500321>
  • Zeller K.-P., Meier H., Müller E.: Untersuchungen zur Wolff-Umlagerung—II. Tetrahedron 1972, 28, 5831. <https://doi.org/10.1016/S0040-4020(01)88926-2>