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Peer-reviewedCC BYChemical Communications

Nitrous oxide-derived vinyldiazotates: structure and reactivity

  • Christeena Mathew
  • Alexandre Genoux
  • Damien Chen
  • Abdusalom Suleymanov
  • Farzaneh Fadaei-Tirani
  • Rosario Scopelliti
  • Kay Severin
Open at sourceDOICite

Abstract

O)][K×(18-crown-6)]. Upon the addition of Grignard reagents, the lithium diazotate is converted into azo olefins in synthetically useful yields.

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Cite

BibTeXRIS
BibTeX
@article{mathew2026nitrous,
  title = {{Nitrous oxide-derived vinyldiazotates: structure and reactivity}},
  author = {Christeena Mathew and Alexandre Genoux and Damien Chen and Abdusalom Suleymanov and Farzaneh Fadaei-Tirani and Rosario Scopelliti and Kay Severin},
  journal = {Chemical Communications},
  year = {2026},
  month = oct,
  doi = {10.1039/d6cc05278a},
  url = {https://hal.science/hal-05787087v1},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Nitrous oxide-derived vinyldiazotates: structure and reactivity
AU  - Christeena Mathew
AU  - Alexandre Genoux
AU  - Damien Chen
AU  - Abdusalom Suleymanov
AU  - Farzaneh Fadaei-Tirani
AU  - Rosario Scopelliti
AU  - Kay Severin
PY  - 2026
DA  - 2026/10/08
JO  - Chemical Communications
DO  - 10.1039/d6cc05278a
UR  - https://hal.science/hal-05787087v1
AB  - O)][K×(18-crown-6)]. Upon the addition of Grignard reagents, the lithium diazotate is converted into azo olefins in synthetically useful yields.
SN  - 1359-7345
SN  - 1364-548X
ER  -