2015
DOI: 10.1002/chin.201545092
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Enantioselective Synthesis of α‐Quaternary Amino Acids by Alkylation of Deprotonated α‐Aminonitriles.

Abstract: Enantioselective Synthesis of -Quaternary Amino Acids by Alkylation of Deprotonated -Aminonitriles. -An -alkylation of deprotonated -amino nitriles, prepared from chiral phenyldioxanamine (I) by Strecker reaction, leads to -quaternary arylglycines with high optical purity after hydrolysis and oxidative cleavage of the chiral auxiliary. The procedure requires only chromatographic purification of the final products. -(NETZ, I.; KUCUKDISLI, M.; OPATZ*, T.; J. Org. Chem. 80 (2015) 13, 6864-6869, http://dx.doi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?