Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction

Igor B. Kutyashev; Maxim S. Sannikov; Ivan A. Kochnev; Alexey Y. Barkov; Nikolay S. Zimnitskiy; Vladislav Y. Korotaev; Vyacheslav Y. Sosnovskikh

doi:10.1055/s-0040-1706005

Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction

Igor B. Kutyashev, Maxim S. Sannikov, Ivan A. Kochnev, Alexey Y. Barkov, Nikolay S. Zimnitskiy, Vladislav Y. Korotaev, Vyacheslav Y. Sosnovskikh

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Original language	English
Article number	so-2020-d0043-op
Pages (from-to)	1-16
Number of pages	16
Journal	Synopen
Volume	5
Issue number	1
DOIs	https://doi.org/10.1055/s-0040-1706005
Publication status	Published - Jan 2021

Keywords

3-nitro-2-trifluoro(trichloro)methyl-2H-chromenes
1,3-dipolar cycloaddition
azomethine ylides
acenaphthenequinone
cyclic.-amino acids
MULTICOMPONENT 1,3-DIPOLAR CYCLOADDITION
STEREOSELECTIVE-SYNTHESIS
AZOMETHINE
3-NITRO-2H-CHROMENES
PROLIFERATION
HETEROCYCLES
DERIVATIVES
CHEMISTRY
APOPTOSIS
PROLINE
cyclic α-amino acids
3-nitro-2-trifluoro(trichloro)methyl- 2H -chromenes

ASJC Scopus subject areas

Catalysis
Biomaterials
Materials Science (miscellaneous)
Organic Chemistry

WoS ResearchAreas Categories

Chemistry, Organic

Access to Document

10.1055/s-0040-1706005

Cite this

Kutyashev, I. B., Sannikov, M. S., Kochnev, I. A., Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., & Sosnovskikh, V. Y. (2021). Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction. Synopen, 5(1), 1-16. [so-2020-d0043-op]. https://doi.org/10.1055/s-0040-1706005

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title = "Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction",

keywords = "3-nitro-2-trifluoro(trichloro)methyl-2H-chromenes, 1,3-dipolar cycloaddition, azomethine ylides, acenaphthenequinone, cyclic.-amino acids, MULTICOMPONENT 1,3-DIPOLAR CYCLOADDITION, STEREOSELECTIVE-SYNTHESIS, AZOMETHINE, 3-NITRO-2H-CHROMENES, PROLIFERATION, HETEROCYCLES, DERIVATIVES, CHEMISTRY, APOPTOSIS, PROLINE, cyclic α-amino acids, 3-nitro-2-trifluoro(trichloro)methyl- 2H -chromenes",

author = "Kutyashev, {Igor B.} and Sannikov, {Maxim S.} and Kochnev, {Ivan A.} and Barkov, {Alexey Y.} and Zimnitskiy, {Nikolay S.} and Korotaev, {Vladislav Y.} and Sosnovskikh, {Vyacheslav Y.}",

year = "2021",

month = jan,

doi = "10.1055/s-0040-1706005",

language = "English",

volume = "5",

pages = "1--16",

journal = "Synopen",

issn = "2509-9396",

publisher = "Georg Thieme Verlag",

number = "1",

}

Kutyashev, IB, Sannikov, MS, Kochnev, IA , Barkov, AY , Zimnitskiy, NS , Korotaev, VY & Sosnovskikh, VY 2021, 'Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction', Synopen, vol. 5, no. 1, so-2020-d0043-op, pp. 1-16. https://doi.org/10.1055/s-0040-1706005

Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction. / Kutyashev, Igor B.; Sannikov, Maxim S.; Kochnev, Ivan A. et al.

In: Synopen, Vol. 5, No. 1, so-2020-d0043-op, 01.2021, p. 1-16.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction

AU - Kutyashev, Igor B.

AU - Sannikov, Maxim S.

AU - Kochnev, Ivan A.

AU - Barkov, Alexey Y.

AU - Zimnitskiy, Nikolay S.

AU - Korotaev, Vladislav Y.

AU - Sosnovskikh, Vyacheslav Y.

PY - 2021/1

Y1 - 2021/1

KW - 3-nitro-2-trifluoro(trichloro)methyl-2H-chromenes

KW - 1,3-dipolar cycloaddition

KW - azomethine ylides

KW - acenaphthenequinone

KW - cyclic.-amino acids

KW - MULTICOMPONENT 1,3-DIPOLAR CYCLOADDITION

KW - STEREOSELECTIVE-SYNTHESIS

KW - AZOMETHINE

KW - 3-NITRO-2H-CHROMENES

KW - PROLIFERATION

KW - HETEROCYCLES

KW - DERIVATIVES

KW - CHEMISTRY

KW - APOPTOSIS

KW - PROLINE

KW - cyclic α-amino acids

KW - 3-nitro-2-trifluoro(trichloro)methyl- 2H -chromenes

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U2 - 10.1055/s-0040-1706005

DO - 10.1055/s-0040-1706005

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EP - 16

JO - Synopen

JF - Synopen

SN - 2509-9396

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M1 - so-2020-d0043-op

ER -

Kutyashev IB, Sannikov MS, Kochnev IA , Barkov AY , Zimnitskiy NS , Korotaev VY et al. Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction. Synopen. 2021 Jan;5(1):1-16. so-2020-d0043-op. https://doi.org/10.1055/s-0040-1706005

Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction

Keywords

ASJC Scopus subject areas

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Карбо- и гетероаннелирование 3-нитро-2-(трифторметил)-2Н-хроменов

New Synthesis Method Developed at UrFU Could Facilitate Production of Anticancer Drugs

В вузе разработали простой метод создания веществ для борьбы с раком

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Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo-addition Reaction

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ASJC Scopus subject areas

WoS ResearchAreas Categories

Access to Document

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Fingerprint

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Карбо- и гетероаннелирование 3-нитро-2-(трифторметил)-2Н-хроменов

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New Synthesis Method Developed at UrFU Could Facilitate Production of Anticancer Drugs

В вузе разработали простой метод создания веществ для борьбы с раком

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