Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles
An acid-assisted [4 + 1]-cycloaddition of indoles with nitrostyrenes affords 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically pure form. Several of these spirocyclic molecules exhibit promising anticancer activity by reducing viability and inducing differentiation of neuroblastoma cells
Salvato in:
Autori principali: | , , , , , , , , , , , |
---|---|
Natura: | Статья |
Lingua: | English |
Pubblicazione: |
American Chemical Society
2019
|
Soggetti: | |
Accesso online: | https://www.scopus.com/record/display.uri?eid=2-s2.0-85067007191&origin=resultslist&sort=plf-f&src=s&st1=Synthesis+of+Spiro%5bindole-3%2c5%E2%80%B2-isoxazoles%5d+with+Anticancer+Activity+via+a+Formal+%5b4+%2b+1%5d-Spirocyclization+of+Nitroalkenes+to+Indoles&st2=&sid=0a6da1faec8406656ad1e7a9ab6c75b0&sot=b&sdt=b&sl=147&s=TITLE-ABS-KEY%28Synthesis+of+Spiro%5bindole-3%2c5%E2%80%B2-isoxazoles%5d+with+Anticancer+Activity+via+a+Formal+%5b4+%2b+1%5d-Spirocyclization+of+Nitroalkenes+to+Indoles%29&relpos=0&citeCnt=0&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/5582 |
Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|
id |
ir-20.500.12258-5582 |
---|---|
record_format |
dspace |
spelling |
ir-20.500.12258-55822020-07-29T11:57:55Z Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles Aksenov, A. V. Аксенов, А. В. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. V. Александрова, Е. В. Rubin, M. A. Рубин, М. А. Anticancer activity Indoles Nitroalkenes Spirocyclization An acid-assisted [4 + 1]-cycloaddition of indoles with nitrostyrenes affords 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically pure form. Several of these spirocyclic molecules exhibit promising anticancer activity by reducing viability and inducing differentiation of neuroblastoma cells 2019-06-25T12:20:31Z 2019-06-25T12:20:31Z 2019 Статья Aksenov, A.V., Aksenov, D.A., Arutiunov, N.A., Aksenov, N.A., Aleksandrova, E.V., Zhao, Z., Du, L., Kornienko, A., Rubin, M. Synthesis of Spiro[indole-3,5′-isoxazoles] with Anticancer Activity via a Formal [4 + 1]-Spirocyclization of Nitroalkenes to Indoles // Journal of Organic Chemistry. - 2019. - Volume 84. - Issue 11. - Pages 7123-7137 https://www.scopus.com/record/display.uri?eid=2-s2.0-85067007191&origin=resultslist&sort=plf-f&src=s&st1=Synthesis+of+Spiro%5bindole-3%2c5%E2%80%B2-isoxazoles%5d+with+Anticancer+Activity+via+a+Formal+%5b4+%2b+1%5d-Spirocyclization+of+Nitroalkenes+to+Indoles&st2=&sid=0a6da1faec8406656ad1e7a9ab6c75b0&sot=b&sdt=b&sl=147&s=TITLE-ABS-KEY%28Synthesis+of+Spiro%5bindole-3%2c5%E2%80%B2-isoxazoles%5d+with+Anticancer+Activity+via+a+Formal+%5b4+%2b+1%5d-Spirocyclization+of+Nitroalkenes+to+Indoles%29&relpos=0&citeCnt=0&searchTerm= http://hdl.handle.net/20.500.12258/5582 en Journal of Organic Chemistry application/pdf application/pdf American Chemical Society |
institution |
СКФУ |
collection |
Репозиторий |
language |
English |
topic |
Anticancer activity Indoles Nitroalkenes Spirocyclization |
spellingShingle |
Anticancer activity Indoles Nitroalkenes Spirocyclization Aksenov, A. V. Аксенов, А. В. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. V. Александрова, Е. В. Rubin, M. A. Рубин, М. А. Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
description |
An acid-assisted [4 + 1]-cycloaddition of indoles with nitrostyrenes affords 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically pure form. Several of these spirocyclic molecules exhibit promising anticancer activity by reducing viability and inducing differentiation of neuroblastoma cells |
format |
Статья |
author |
Aksenov, A. V. Аксенов, А. В. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. V. Александрова, Е. В. Rubin, M. A. Рубин, М. А. |
author_facet |
Aksenov, A. V. Аксенов, А. В. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. V. Александрова, Е. В. Rubin, M. A. Рубин, М. А. |
author_sort |
Aksenov, A. V. |
title |
Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
title_short |
Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
title_full |
Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
title_fullStr |
Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
title_full_unstemmed |
Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
title_sort |
synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles |
publisher |
American Chemical Society |
publishDate |
2019 |
url |
https://www.scopus.com/record/display.uri?eid=2-s2.0-85067007191&origin=resultslist&sort=plf-f&src=s&st1=Synthesis+of+Spiro%5bindole-3%2c5%E2%80%B2-isoxazoles%5d+with+Anticancer+Activity+via+a+Formal+%5b4+%2b+1%5d-Spirocyclization+of+Nitroalkenes+to+Indoles&st2=&sid=0a6da1faec8406656ad1e7a9ab6c75b0&sot=b&sdt=b&sl=147&s=TITLE-ABS-KEY%28Synthesis+of+Spiro%5bindole-3%2c5%E2%80%B2-isoxazoles%5d+with+Anticancer+Activity+via+a+Formal+%5b4+%2b+1%5d-Spirocyclization+of+Nitroalkenes+to+Indoles%29&relpos=0&citeCnt=0&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/5582 |
work_keys_str_mv |
AT aksenovav synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aksenovav synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aksenovda synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aksenovda synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT arutiunovna synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT arutûnovna synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aksenovna synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aksenovna synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aleksandrovaev synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT aleksandrovaev synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT rubinma synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles AT rubinma synthesisofspiroindole35isoxazoleswithanticanceractivityviaaformal41spirocyclizationofnitroalkenestoindoles |
_version_ |
1760600318553358336 |