Tags

Type your tag names separated by a space and hit enter

Organocatalytic chemoselective asymmetric N-allylic alkylation of enamides.
Chem Commun (Camb). 2011 Apr 28; 47(16):4784-6.CC

Abstract

The first Lewis base-catalysed chemoselective asymmetric N-allylic alkylation of enamides with Morita-Baylis-Hillman carbonates has been developed, which affords multifunctional products in moderate to high enantioselectivity (up to 92% ee).

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Huang JR
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Cui HL
No affiliation info available
Lei J
No affiliation info available
Sun XH
No affiliation info available
Chen YC
No affiliation info available

MeSH

AlkylationAmidesCatalysisLewis BasesMolecular StructureStereoisomerism

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21409282

Citation

Huang, Ji-Rong, et al. "Organocatalytic Chemoselective Asymmetric N-allylic Alkylation of Enamides." Chemical Communications (Cambridge, England), vol. 47, no. 16, 2011, pp. 4784-6.
Huang JR, Cui HL, Lei J, et al. Organocatalytic chemoselective asymmetric N-allylic alkylation of enamides. Chem Commun (Camb). 2011;47(16):4784-6.
Huang, J. R., Cui, H. L., Lei, J., Sun, X. H., & Chen, Y. C. (2011). Organocatalytic chemoselective asymmetric N-allylic alkylation of enamides. Chemical Communications (Cambridge, England), 47(16), 4784-6. https://doi.org/10.1039/c0cc05616b
Huang JR, et al. Organocatalytic Chemoselective Asymmetric N-allylic Alkylation of Enamides. Chem Commun (Camb). 2011 Apr 28;47(16):4784-6. PubMed PMID: 21409282.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Organocatalytic chemoselective asymmetric N-allylic alkylation of enamides. AU - Huang,Ji-Rong, AU - Cui,Hai-Lei, AU - Lei,Jie, AU - Sun,Xun-Hao, AU - Chen,Ying-Chun, Y1 - 2011/03/16/ PY - 2011/3/17/entrez PY - 2011/3/17/pubmed PY - 2011/7/29/medline SP - 4784 EP - 6 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 47 IS - 16 N2 - The first Lewis base-catalysed chemoselective asymmetric N-allylic alkylation of enamides with Morita-Baylis-Hillman carbonates has been developed, which affords multifunctional products in moderate to high enantioselectivity (up to 92% ee). SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/21409282/Organocatalytic_chemoselective_asymmetric_N_allylic_alkylation_of_enamides_ L2 - https://doi.org/10.1039/c0cc05616b DB - PRIME DP - Unbound Medicine ER -