Access to Enantioenriched Spiro‐ ϵ ‐Lactam Oxindoles by an N‐Heterocyclic Carbene‐Catalyzed [4+3] Annulation of Flexible Oxotryptamines with Enals-Reference-Cited by-同舟云学术

Access to Enantioenriched Spiro‐ ϵ ‐Lactam Oxindoles by an N‐Heterocyclic Carbene‐Catalyzed [4+3] Annulation of Flexible Oxotryptamines with Enals

Published:2019-08 Issue: Volume: Page:
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Liu Dehai¹,Hu Zhouli¹,Zhang Yuxia¹,Gong Minghua¹,Fu Zhenqian¹²^ORCID,Huang Wei¹²

Affiliation:

1. Key Laboratory of Flexible Electronics & Institute of Advanced MaterialsJiangsu National Synergetic Innovation Center for Advanced MaterialsNanjing Tech University 30 South Puzhu Road Nanjing 211816 P. R. China

2. Shaanxi Institute of Flexible Electronics (SIFE)Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 P. R. China

Funder

Key Technologies Research and Development Program

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201903144

Reference116 articles.

1. For selected reviews see:

2. Nucleophilic Carbenes in Asymmetric Organocatalysis

3. Organocatalysis by N-Heterocyclic Carbenes

4. Employing homoenolates generated by NHC catalysis in carbon–carbon bond-forming reactions: state of the art

5. NHCs in Asymmetric Organocatalysis: Recent Advances in Azolium Enolate Generation and Reactivity

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