Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation.Angew Chem Int Ed Engl. 2006 Apr 03; 45(15):2466-9.AC
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
16526068
Citation
Schelwies, Mathias, et al. "Enantioselective Modular Synthesis of 2,4-disubstituted Cyclopentenones By Iridium-catalyzed Allylic Alkylation." Angewandte Chemie (International Ed. in English), vol. 45, no. 15, 2006, pp. 2466-9.
Schelwies M, Dübon P, Helmchen G. Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation. Angew Chem Int Ed Engl. 2006;45(15):2466-9.
Schelwies, M., Dübon, P., & Helmchen, G. (2006). Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation. Angewandte Chemie (International Ed. in English), 45(15), 2466-9.
Schelwies M, Dübon P, Helmchen G. Enantioselective Modular Synthesis of 2,4-disubstituted Cyclopentenones By Iridium-catalyzed Allylic Alkylation. Angew Chem Int Ed Engl. 2006 Apr 3;45(15):2466-9. PubMed PMID: 16526068.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation.
AU - Schelwies,Mathias,
AU - Dübon,Pierre,
AU - Helmchen,Günter,
PY - 2006/3/10/pubmed
PY - 2007/5/23/medline
PY - 2006/3/10/entrez
SP - 2466
EP - 9
JF - Angewandte Chemie (International ed. in English)
JO - Angew Chem Int Ed Engl
VL - 45
IS - 15
SN - 1433-7851
UR - https://www.unboundmedicine.com/medline/citation/16526068/Enantioselective_modular_synthesis_of_24_disubstituted_cyclopentenones_by_iridium_catalyzed_allylic_alkylation_
DB - PRIME
DP - Unbound Medicine
ER -