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.
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 -