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A new chiral catalyst for the enantioselective Strecker synthesis of alpha-amino acids.
Org Lett. 2004 Dec 23; 6(26):5027-9.OL

Abstract

[reaction: see text] The chiral ammonium salt 3 is demonstrated to be an effective catalyst for the highly enantioselective Strecker reaction of N-allylbenzaldimines with hydrogen cyanide in CH2Cl2 solution.

Authors+Show Affiliations

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

15606127

Citation

Huang, Jinkun, and E J. Corey. "A New Chiral Catalyst for the Enantioselective Strecker Synthesis of Alpha-amino Acids." Organic Letters, vol. 6, no. 26, 2004, pp. 5027-9.
Huang J, Corey EJ. A new chiral catalyst for the enantioselective Strecker synthesis of alpha-amino acids. Org Lett. 2004;6(26):5027-9.
Huang, J., & Corey, E. J. (2004). A new chiral catalyst for the enantioselective Strecker synthesis of alpha-amino acids. Organic Letters, 6(26), 5027-9.
Huang J, Corey EJ. A New Chiral Catalyst for the Enantioselective Strecker Synthesis of Alpha-amino Acids. Org Lett. 2004 Dec 23;6(26):5027-9. PubMed PMID: 15606127.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A new chiral catalyst for the enantioselective Strecker synthesis of alpha-amino acids. AU - Huang,Jinkun, AU - Corey,E J, PY - 2004/12/21/pubmed PY - 2006/5/23/medline PY - 2004/12/21/entrez SP - 5027 EP - 9 JF - Organic letters JO - Org Lett VL - 6 IS - 26 N2 - [reaction: see text] The chiral ammonium salt 3 is demonstrated to be an effective catalyst for the highly enantioselective Strecker reaction of N-allylbenzaldimines with hydrogen cyanide in CH2Cl2 solution. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/15606127/A_new_chiral_catalyst_for_the_enantioselective_Strecker_synthesis_of_alpha_amino_acids_ DB - PRIME DP - Unbound Medicine ER -