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Intramolecular Oxa-Michael Reactions of Aldols Generated from Enones and Isatins to Afford Spirooxindole Tetrahydropyrans

https://oist.repo.nii.ac.jp/records/1177
https://oist.repo.nii.ac.jp/records/1177
1bf2c5a7-5676-49c7-85f1-00b5894915d3
Name / File License Actions
COM-19-S(F)26.pdf COM-19-S(F)26 (624.8 kB)
Heterocycles2020,101,339sup_COM-19-S(F)26_SI.pdf Heterocycles2020,101,339sup_COM-19-S(F)26_SI.pdf (6.1 MB)
Item type 学術雑誌論文 / Journal Article(1)
PubDate 2020-02-17
Title
Title Intramolecular Oxa-Michael Reactions of Aldols Generated from Enones and Isatins to Afford Spirooxindole Tetrahydropyrans
Language en
Language
Language eng
Resource Type
Resource Type Identifier http://purl.org/coar/resource_type/c_6501
Resource Type journal article
Access Right
Access Rights open access
Access Rights URI http://purl.org/coar/access_right/c_abf2
Author Pasha, Maira

× Pasha, Maira

Pasha, Maira

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Sohail, Muhammad

× Sohail, Muhammad

Sohail, Muhammad

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Tanaka, Fujie

× Tanaka, Fujie

Tanaka, Fujie

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Bibliographic Information en : HETEROCYCLES

Volume Number 101, Issue Number 1, p. 339-346, Issue Date 2019-08-07
Abstract
Description Type Other
Description Spirooxindole derivatives are found in bioactive natural products and are used in drug discovery and related research. Here, acid-catalyzed diastereoselective intramolecular oxa-Michael cyclization reactions of β-hydroxyenones generated from enones and isatin derivatives that afford spirooxindole tetrahydropyranes are reported. The major diastereomers of the products of these reactions were previously difficult to access by the amine-catalyzed hetero-Diels-Alder reactions of enones with isatins. With the use of enantiomerically enriched forms of the starting materials in the reactions, enantiomerically enriched spirooxindole tetrahydropyranes that retained the enantiopurities of the starting materials were obtained.
Publisher
Publisher The Japan Institute of Heterocyclic Chemistry Publications
ISSN
Source Identifier Type ISSN
Source Identifier 1881-0942
DOI
Relation Type isIdenticalTo
Identifier Type DOI
Related Identifier info:doi/10.3987/COM-19-S(F)26
Rights
Rights © 2020 The Japan Institute of Heterocyclic Chemistry
Related site
Identifier Type URI
Related Identifier https://www.heterocycles.jp/newlibrary/libraries/search
Author's flag
Version Type VoR
Version Type Resource http://purl.org/coar/version/c_970fb48d4fbd8a85
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