Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles

Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles

10.1039/c9qo00471h

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Main Authors: Zhang, Jing, Chan, Wai-Lun, Chen, Ligong, Ullah, Nisar, Lu, Yixin
Other Authors: CHEMISTRY
Format: Article
Language:English
Published: ROYAL SOC CHEMISTRY 2020
Subjects:
Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
MICHAEL ADDITION
CONSTRUCTION
CASCADE
ALLENES
SPIROOXINDOLES
ALLENOATES
DISCOVERY
KETIMINES
DESIGN
POTENT
Online Access:https://scholarbank.nus.edu.sg/handle/10635/169692
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Institution: National University of Singapore
Language: English
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spelling sg-nus-scholar.10635-1696922024-11-08T19:35:02Z Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles Zhang, Jing Chan, Wai-Lun Chen, Ligong Ullah, Nisar Lu, Yixin CHEMISTRY Prof Lu Yixin Science & Technology Physical Sciences Chemistry, Organic Chemistry MICHAEL ADDITION CONSTRUCTION CASCADE ALLENES SPIROOXINDOLES ALLENOATES DISCOVERY KETIMINES DESIGN POTENT 10.1039/c9qo00471h ORGANIC CHEMISTRY FRONTIERS 6 13 2210-2214 2020-06-12T00:55:16Z 2020-06-12T00:55:16Z 2019-07-07 2020-06-04T04:51:14Z Article Zhang, Jing, Chan, Wai-Lun, Chen, Ligong, Ullah, Nisar, Lu, Yixin (2019-07-07). Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles. ORGANIC CHEMISTRY FRONTIERS 6 (13) : 2210-2214. ScholarBank@NUS Repository. https://doi.org/10.1039/c9qo00471h 20524129 https://scholarbank.nus.edu.sg/handle/10635/169692 en ROYAL SOC CHEMISTRY Elements
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
language English
topic Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
MICHAEL ADDITION
CONSTRUCTION
CASCADE
ALLENES
SPIROOXINDOLES
ALLENOATES
DISCOVERY
KETIMINES
DESIGN
POTENT
spellingShingle Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
MICHAEL ADDITION
CONSTRUCTION
CASCADE
ALLENES
SPIROOXINDOLES
ALLENOATES
DISCOVERY
KETIMINES
DESIGN
POTENT
Zhang, Jing
Chan, Wai-Lun
Chen, Ligong
Ullah, Nisar
Lu, Yixin
Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles
description 10.1039/c9qo00471h
author2 CHEMISTRY
author_facet CHEMISTRY
Zhang, Jing
Chan, Wai-Lun
Chen, Ligong
Ullah, Nisar
Lu, Yixin
format Article
author Zhang, Jing
Chan, Wai-Lun
Chen, Ligong
Ullah, Nisar
Lu, Yixin
author_sort Zhang, Jing
title Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles
title_short Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles
title_full Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles
title_fullStr Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles
title_full_unstemmed Creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the Morita-Baylis-Hillman carbonates with pyrazoloneyldiene oxindoles
title_sort creation of bispiro[pyrazolone-3,3 '-oxindoles] via a phosphine-catalyzed enantioselective [3+2] annulation of the morita-baylis-hillman carbonates with pyrazoloneyldiene oxindoles
publisher ROYAL SOC CHEMISTRY
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/169692
_version_ 1821230129835147264

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