Self-Assembled Bio-Organometallic Nanocatalysts for Highly Enantioselective Direct Aldol Reactions-Reference-Cited by-同舟云学术

Self-Assembled Bio-Organometallic Nanocatalysts for Highly Enantioselective Direct Aldol Reactions

Published:2020-11-11 Issue:46 Volume:36 Page:13735-13742
ISSN:0743-7463
Container-title:Langmuir
language:en
Short-container-title:Langmuir

Author:

Yang Xuejiao¹,Zhang Liwei¹,Liang Yaoyu¹,Wang Yuefei¹²^ORCID,Shen Yuhe¹,Xing Qiguo¹,Qi Wei¹³²^ORCID,Wang Pengfei⁴,Liu Xiao¹^ORCID,Yang Mengyao¹,Su Rongxin¹³²^ORCID,He Mingxia⁴,He Zhimin¹

Affiliation:

1. State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, P. R. China

2. Tianjin Key Laboratory of Membrane Science and Desalination Technology, Tianjin University, Tianjin 300072, P. R. China

3. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. China

4. State Key Laboratory of Precision Measuring Technology and Instruments, Tianjin University, Tianjin 30072, P. R. China

Funder

State Key Laboratory of Chemical Engineering

National Natural Science Foundation of China

Tianjin Development Program for Innovation and Entrepreneurship

Publisher

American Chemical Society (ACS)

Subject

Electrochemistry,Spectroscopy,Surfaces and Interfaces,Condensed Matter Physics,General Materials Science

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.langmuir.0c01485

Reference48 articles.

1. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures

2. Asymmetric synthesis of bicyclic intermediates of natural product chemistry

3. Proline-Catalyzed Direct Asymmetric Aldol Reactions

4. Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions

5. Proline-catalyzed asymmetric assembly reactions: enzyme-like assembly of carbohydrates and polyketides from three aldehyde substrates

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