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Chiral primary-secondary diamines catalyzed Michael-aldol-dehydration reaction between benzoylacetates and alpha,beta-unsaturated ketones: highly enantioselective synthesis of functionalized chiral cyclohexenones.
Chemistry. 2009 Dec 14; 15(48):13295-8.C

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Publisher Full Text (DOI)

Authors+Show Affiliations

Yang YQ
Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.
Chai Z
No affiliation info available
Wang HF
No affiliation info available
Chen XK
No affiliation info available
Cui HF
No affiliation info available
Zheng CW
No affiliation info available
Xiao H
No affiliation info available
Li P
No affiliation info available
Zhao G
No affiliation info available

MeSH

AcetatesBenzeneCatalysisCyclohexanonesDiaminesKetonesMolecular StructureStereoisomerism

Pub Type(s)

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

Language

eng

PubMed ID

19908264

Citation

Yang, Ying-Quan, et al. "Chiral Primary-secondary Diamines Catalyzed Michael-aldol-dehydration Reaction Between Benzoylacetates and Alpha,beta-unsaturated Ketones: Highly Enantioselective Synthesis of Functionalized Chiral Cyclohexenones." Chemistry (Weinheim an Der Bergstrasse, Germany), vol. 15, no. 48, 2009, pp. 13295-8.
Yang YQ, Chai Z, Wang HF, et al. Chiral primary-secondary diamines catalyzed Michael-aldol-dehydration reaction between benzoylacetates and alpha,beta-unsaturated ketones: highly enantioselective synthesis of functionalized chiral cyclohexenones. Chemistry. 2009;15(48):13295-8.
Yang, Y. Q., Chai, Z., Wang, H. F., Chen, X. K., Cui, H. F., Zheng, C. W., Xiao, H., Li, P., & Zhao, G. (2009). Chiral primary-secondary diamines catalyzed Michael-aldol-dehydration reaction between benzoylacetates and alpha,beta-unsaturated ketones: highly enantioselective synthesis of functionalized chiral cyclohexenones. Chemistry (Weinheim an Der Bergstrasse, Germany), 15(48), 13295-8. https://doi.org/10.1002/chem.200901541
Yang YQ, et al. Chiral Primary-secondary Diamines Catalyzed Michael-aldol-dehydration Reaction Between Benzoylacetates and Alpha,beta-unsaturated Ketones: Highly Enantioselective Synthesis of Functionalized Chiral Cyclohexenones. Chemistry. 2009 Dec 14;15(48):13295-8. PubMed PMID: 19908264.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Chiral primary-secondary diamines catalyzed Michael-aldol-dehydration reaction between benzoylacetates and alpha,beta-unsaturated ketones: highly enantioselective synthesis of functionalized chiral cyclohexenones. AU - Yang,Ying-Quan, AU - Chai,Zhuo, AU - Wang,Hai-Feng, AU - Chen,Xing-Kuan, AU - Cui,Hai-Feng, AU - Zheng,Chang-Wu, AU - Xiao,Hua, AU - Li,Peng, AU - Zhao,Gang, PY - 2009/11/13/entrez PY - 2009/11/13/pubmed PY - 2010/3/2/medline SP - 13295 EP - 8 JF - Chemistry (Weinheim an der Bergstrasse, Germany) JO - Chemistry VL - 15 IS - 48 SN - 1521-3765 UR - https://www.unboundmedicine.com/medline/citation/19908264/Chiral_primary_secondary_diamines_catalyzed_Michael_aldol_dehydration_reaction_between_benzoylacetates_and_alphabeta_unsaturated_ketones:_highly_enantioselective_synthesis_of_functionalized_chiral_cyclohexenones_ L2 - https://doi.org/10.1002/chem.200901541 DB - PRIME DP - Unbound Medicine ER -