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Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles. / Ростовский, Николай Витальевич; Новиков, Михаил Сергеевич.

Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications. Wiley-Blackwell, 2025. p. 83-114.

Research output: Chapter in Book/Report/Conference proceedingChapterResearchpeer-review

Harvard

Ростовский, НВ & Новиков, МС 2025, Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles. in Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications. Wiley-Blackwell, pp. 83-114. https://doi.org/10.1002/9783527844852.ch4

APA

Ростовский, Н. В., & Новиков, М. С. (2025). Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles. In Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications (pp. 83-114). Wiley-Blackwell. https://doi.org/10.1002/9783527844852.ch4

Vancouver

Ростовский НВ, Новиков МС. Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles. In Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications. Wiley-Blackwell. 2025. p. 83-114 https://doi.org/10.1002/9783527844852.ch4

Author

Ростовский, Николай Витальевич ; Новиков, Михаил Сергеевич. / Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles. Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications. Wiley-Blackwell, 2025. pp. 83-114

BibTeX

@inbook{2ad1f7807e59435ebb21e1ca96aefa01,
title = "Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles",
abstract = "This chapter presents a general analysis of the transannulations of 1-sulfonyl-1,2,3-triazoles with cyclic substrates with an emphasis on advances in recent years in this field. These transannulation reactions can occur either with the retention of the ring of the substrate, providing fused heterocyclic systems, or its opening, which generates a variety of unique heterocycles of various sizes and constituents. Future perspectives in this field are also discussed.",
keywords = "azavinylcarbene, heterocycle, rhodium, ring-opening, transannulation, ylide",
author = "Ростовский, {Николай Витальевич} and Новиков, {Михаил Сергеевич}",
year = "2025",
month = jan,
day = "1",
doi = "10.1002/9783527844852.ch4",
language = "English",
isbn = "9783527353163",
pages = "83--114",
booktitle = "Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications",
publisher = "Wiley-Blackwell",
address = "United States",

}

RIS

TY - CHAP

T1 - Transannulations of N-Sulfonyl-1,2,3-triazoles with Carbo/Heterocycles

AU - Ростовский, Николай Витальевич

AU - Новиков, Михаил Сергеевич

PY - 2025/1/1

Y1 - 2025/1/1

N2 - This chapter presents a general analysis of the transannulations of 1-sulfonyl-1,2,3-triazoles with cyclic substrates with an emphasis on advances in recent years in this field. These transannulation reactions can occur either with the retention of the ring of the substrate, providing fused heterocyclic systems, or its opening, which generates a variety of unique heterocycles of various sizes and constituents. Future perspectives in this field are also discussed.

AB - This chapter presents a general analysis of the transannulations of 1-sulfonyl-1,2,3-triazoles with cyclic substrates with an emphasis on advances in recent years in this field. These transannulation reactions can occur either with the retention of the ring of the substrate, providing fused heterocyclic systems, or its opening, which generates a variety of unique heterocycles of various sizes and constituents. Future perspectives in this field are also discussed.

KW - azavinylcarbene

KW - heterocycle

KW - rhodium

KW - ring-opening

KW - transannulation

KW - ylide

UR - https://www.mendeley.com/catalogue/1d9a6f80-f95e-398e-8d56-43326780f41f/

U2 - 10.1002/9783527844852.ch4

DO - 10.1002/9783527844852.ch4

M3 - Chapter

SN - 9783527353163

SP - 83

EP - 114

BT - Denitrogenative Transformation of Nitrogen Heterocycles: Synthesis, Reactions and Applications

PB - Wiley-Blackwell

ER -

ID: 127697655