ChemInform Abstract: Highly Enantioselective Chlorination of β‐Keto Esters and Subsequent S<sub>N</sub>2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers.

Shibatomi, Kazutaka; Soga, Yoshinori; Narayama, Akira; Fujisawa, Ikuhide; Iwasa, Seiji

doi:10.1002/chin.201245029

ChemInform

2012

DOI: 10.1002/chin.201245029

|View full text |Cite

ChemInform Abstract: Highly Enantioselective Chlorination of β‐Keto Esters and Subsequent S_N2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers.

Kazutaka Shibatomi

Yoshinori Soga

Akira Narayama

et al.

Abstract: The reaction occurs in the presence of the new ligands (I) affording α‐chlorinated products with high enantioselectivity.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Publication Types

Select...

Relationship

Self Cite0

Independent0

Authors

Journals

Cited by 0 publications

References 1 publication

Supporting

Mentioning

Contrasting

Order By: Relevance

No citations

Set email alert for when this publication receives citations?

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

hi@scite.ai

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

ChemInform Abstract: Highly Enantioselective Chlorination of β‐Keto Esters and Subsequent S_N2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers.

Abstract: The reaction occurs in the presence of the new ligands (I) affording α‐chlorinated products with high enantioselectivity.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Highly Enantioselective Chlorination of β‐Keto Esters and Subsequent SN2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers.

Abstract: The reaction occurs in the presence of the new ligands (I) affording α‐chlorinated products with high enantioselectivity.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Highly Enantioselective Chlorination of β‐Keto Esters and Subsequent S_N2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers.