Diastereodivergent Asymmetric Michael Addition of Cyclic Azomethine Ylides to Nitroalkenes: Direct Approach for the Synthesis of 1,7‐Diazaspiro[4.4]nonane Diastereoisomers-Reference-Cited by-同舟云学术

Diastereodivergent Asymmetric Michael Addition of Cyclic Azomethine Ylides to Nitroalkenes: Direct Approach for the Synthesis of 1,7‐Diazaspiro[4.4]nonane Diastereoisomers

Published:2015-11-16 Issue:52 Volume:21 Page:19048-19057
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Li Chun‐Yan¹,Yang Wu‐Lin¹,Luo Xiaoyan¹,Deng Wei‐Ping¹

Affiliation:

1. Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of, Science and Technology, 130 Meilong Road, Shanghai 200237 (P.R. China)

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201503729

Reference93 articles.

2. Axially Chiral Spirosilanes via Catalytic Asymmetric Intramolecular Hydrosilation

3. Stereocontrolled synthesis of spirocyclics

4. A synthon approach to spiro compounds

5. Spiro Skeletons: A Class of Privileged Structure for Chiral Ligand Design

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