Download PDF
CC BY 4.0 · SynOpen 2023; 07(01): 110-113
DOI: 10.1055/a-2038-6055
spotlight

Ethyl Diazoacetate

Gabriel A. S. Aquino  ∗
a   Laboratory of Organic Synthesis and Biological Prospecting, Chemistry Institute, Universidade Federal do Rio de Janeiro, Avenida Athos da Silveira Ramos, nº 149, Bloco A, 7º andar, Centro de Tecnologia, Cidade Universitária, Rio de Janeiro, RJ, 21941-909, Brasil
,
Floriano P. Silva-Jr
b   Laboratory of Experimental and Computational Biochemistry of Drugs, Oswaldo Cruz Institute, Fiocruz, Avenida Brasil, nº 4365, Pavilhão Leonidas Deane, Sl. 309, Rio de Janeiro, RJ, 21040-900, Brasil
,
Sabrina B. Ferreira 
a   Laboratory of Organic Synthesis and Biological Prospecting, Chemistry Institute, Universidade Federal do Rio de Janeiro, Avenida Athos da Silveira Ramos, nº 149, Bloco A, 7º andar, Centro de Tecnologia, Cidade Universitária, Rio de Janeiro, RJ, 21941-909, Brasil
› Author Affiliations
› Further Information
   Permissions and Reprints All articles of this category


Abstract

Key words

ethyl diazoacetate - cyclopropanation - pyrazoline - pyrazole - 1,2-rearrangement


Publication History

Received: 02 January 2023

Accepted after revision: 20 February 2023

Accepted Manuscript online:
20 February 2023

Article published online:
08 March 2023

© 2023. This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 

  • References

  • 1 Van Dyke AR, Jamison TF. In Encyclopedia of Reagents for Organic Synthesis, 2nd ed. Paquette LA, Crich D, Fuchs P, Molander G. Wiley; New York: 2009: 2
    Google Scholar
  • 2 Leão RA. C, Ferreira VF, Pinheiro S. Quim. Nova 2007; 30: 1721
    Crossref
  • 3 Caballero A, Prietro A, Díaz-Requejo M, Pérez P. Eur. J. Inorg. Chem. 2009; 9: 1137
    Crossref
  • 4 Dehbanipour Z, Moghadam M, Tangestaninejad S, Mirkhani V, Mohammadpoor-Baltork I. J. Iran. Chem. Soc. 2022; 19: 3371
    Crossref
  • 5 Wu W, Lin Z, Jiang H. Org. Biomol. Chem. 2018; 16: 7315
    CrossrefPubMed
  • 6 Langletz T, Empel C, Jana S, Koenigs R. Tetrahedron Chem. 2022; 3: 100024
    Crossref
  • 7 Zou H, Yang H, Liu Z, Mahmood M, Mei G, Liu H, Chang C. Organometallics 2015; 34: 2791
    Crossref
  • 8 Abeykoon B, Devic T, Grenèche J, Fateeva A, Sorokin AB. Chem. Commun. 2018; 54: 10308
    CrossrefPubMed
  • 9 Rahaman M, Ali MS, Jahan K, Hinz D, Belayet JB, Majinski R, Hossain MM. J. Org. Chem. 2021; 86, 6138
    PubMed
  • 10 Sandeep K, Kumar AS, Qureshi AA, Swamy KC. K. Synthesis. 2022; 54: 4111
    Article in Thieme Connect
  • 11 Balou J, Khalilzadeh MA, Zareyee D. Catal. Lett. 2017; 147: 2612
    Crossref
  • 12 Carreras J, Caballero A, Perez PJ. Angew. Chem. Int. Ed. 2018; 57: 2334
    CrossrefPubMed
  • 13 Cressy D, Zavala C, Abshire A, Sheffield W, Darko A. Dalton Trans. 2020; 49: 15779
    CrossrefPubMed
  • 14 Bykova LS, Kochnev IA, Barkov AY, Zimnitskiy NS, Korotaev VY, Sosnovskikh VY. Chem. Heterocycl. Compd. 2022; 58: 646
    Crossref
  • 15 Chernyak N, Gevorgyan V. Angew. Chem. 2010; 122: 2803
    Crossref
  • 16 Bhattacharjee S, Laru S, Samanta S, Singsardar M, Hajra A. RSC. Adv. 2020; 10: 27984
    CrossrefPubMed
  • 17 Yasukawa T, Kume S, Yamashita Y, Kobayashi S. Chem. Lett. 2021; 50: 1733
    Crossref