Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins--a rational approach.Angew Chem Int Ed Engl. 2008; 47(10):1871-4.AC
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Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
18228232
Citation
Wiesner, Markus, et al. "Tripeptides as Efficient Asymmetric Catalysts for 1,4-addition Reactions of Aldehydes to Nitroolefins--a Rational Approach." Angewandte Chemie (International Ed. in English), vol. 47, no. 10, 2008, pp. 1871-4.
Wiesner M, Revell JD, Wennemers H. Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins--a rational approach. Angew Chem Int Ed Engl. 2008;47(10):1871-4.
Wiesner, M., Revell, J. D., & Wennemers, H. (2008). Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins--a rational approach. Angewandte Chemie (International Ed. in English), 47(10), 1871-4. https://doi.org/10.1002/anie.200704972
Wiesner M, Revell JD, Wennemers H. Tripeptides as Efficient Asymmetric Catalysts for 1,4-addition Reactions of Aldehydes to Nitroolefins--a Rational Approach. Angew Chem Int Ed Engl. 2008;47(10):1871-4. PubMed PMID: 18228232.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins--a rational approach.
AU - Wiesner,Markus,
AU - Revell,Jefferson D,
AU - Wennemers,Helma,
PY - 2008/1/30/pubmed
PY - 2008/4/11/medline
PY - 2008/1/30/entrez
SP - 1871
EP - 4
JF - Angewandte Chemie (International ed. in English)
JO - Angew Chem Int Ed Engl
VL - 47
IS - 10
SN - 1521-3773
UR - https://www.unboundmedicine.com/medline/citation/18228232/Tripeptides_as_efficient_asymmetric_catalysts_for_14_addition_reactions_of_aldehydes_to_nitroolefins__a_rational_approach_
DB - PRIME
DP - Unbound Medicine
ER -