# Highly Enantioselective Catalytic Fluorination and Chlorination Reactions of Carbonyl Compounds Capable of Two‐Point Binding

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/highly-enantioselective-catalytic-fluorination-and-chlorination-reactions-of/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Norio Shibata,Junji Kohno,Kazumi Takai,Takehisa Ishimaru,Shuichi Nakamura,Takeshi Toru,Shuji Kanemasa |
| Citations | 328 |
| DOI | 10.1002/anie.200501041 |
| Fields | Chemistry,Pharmacology, Toxicology and Pharmaceutics |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/anie.200501041 |
| OpenAlex ID | https://openalex.org/W2019445932 |
| PMID | 15942966 |
| Type | article |
| Year | 2005 |

## Paper authors

- [Norio Shibata](https://scholariq.org/researchers/norio-shibata/)

## Paper primary topic

- [Fluorine in Organic Chemistry](https://scholariq.org/topics/fluorine-in-organic-chemistry/)

## Paper topics

- [Fluorine in Organic Chemistry](https://scholariq.org/topics/fluorine-in-organic-chemistry/)
- [Catalytic C–H Functionalization Methods](https://scholariq.org/topics/catalytic-c-h-functionalization-methods/)
- [Cyclopropane Reaction Mechanisms](https://scholariq.org/topics/cyclopropane-reaction-mechanisms/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.