- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Automatic Translation feature is available on CiNii Labs
- Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
BINOL-derived bifunctional sulfide catalysts for asymmetric synthesis of 3,3-disubstituted phthalides via bromolactonization
Search this article
Description
An efficient enantioselective synthesis of 3,3-disubstituted phthalides possessing a chiral quaternary carbon center was achieved via catalytic asymmetric bromolactonization that utilized BINOL-derived bifunctional sulfide catalysts. Transformations of the bromo group in optically active phthalide products were also performed to demonstrate the utility of this novel synthetic protocol.
Journal
-
- Organic & Biomolecular Chemistry
-
Organic & Biomolecular Chemistry 17 (15), 3747-3751, 2019-04-21
Royal Society of Chemistry
- Tweet
Details 詳細情報について
-
- CRID
- 1050005822275593856
-
- NII Article ID
- 120006987740
-
- ISSN
- 14770520
- 14770539
-
- HANDLE
- 10069/39180
-
- PubMed
- 30931456
-
- Text Lang
- en
-
- Article Type
- journal article
-
- Data Source
-
- IRDB
- Crossref
- CiNii Articles
- KAKEN
- OpenAIRE