Domino Reactions through Recursive Anionic Cascades: The Advantageous Use of Nitronates

Publication type: Journal Article
Publication date: 2022-09-23
Wiley
scimago Q2
wos Q2
SJR: 0.558
CiteScore: 4.3
Impact factor: 2.7
ISSN: 1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Abstract
The evolving landscape of recursive nitronate cyclization, as a mechanistically distinct domino strategy employing nitroalkanes as dual-acting one-carbon lynchpins, is discussed in this review. Its advantageous use in rapid assembly of topologically diverse and functionally embellished carbo- and heterocycles is highlighted along with their applications in complex natural products synthesis.
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GOST Copy
Sengupta S., Srihari P., Mehta G. Domino Reactions through Recursive Anionic Cascades: The Advantageous Use of Nitronates // European Journal of Organic Chemistry. 2022.
GOST all authors (up to 50) Copy
Sengupta S., Srihari P., Mehta G. Domino Reactions through Recursive Anionic Cascades: The Advantageous Use of Nitronates // European Journal of Organic Chemistry. 2022.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1002/ejoc.202200945
UR - https://doi.org/10.1002/ejoc.202200945
TI - Domino Reactions through Recursive Anionic Cascades: The Advantageous Use of Nitronates
T2 - European Journal of Organic Chemistry
AU - Sengupta, Saumitra
AU - Srihari, P.
AU - Mehta, Goverdhan
PY - 2022
DA - 2022/09/23
PB - Wiley
SN - 1434-193X
SN - 1099-0690
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2022_Sengupta,
author = {Saumitra Sengupta and P. Srihari and Goverdhan Mehta},
title = {Domino Reactions through Recursive Anionic Cascades: The Advantageous Use of Nitronates},
journal = {European Journal of Organic Chemistry},
year = {2022},
publisher = {Wiley},
month = {sep},
url = {https://doi.org/10.1002/ejoc.202200945},
doi = {10.1002/ejoc.202200945}
}
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