Stereoselective Synthesis of 2,8-Dioxabicyclo[3.3.1]nonane Derivatives via a Sequential Michael Addition/Bicyclization Reaction-Reference-Cited by-同舟云学术

Stereoselective Synthesis of 2,8-Dioxabicyclo[3.3.1]nonane Derivatives via a Sequential Michael Addition/Bicyclization Reaction

Published:2013-03-19 Issue:7 Volume:78 Page:3132-3141
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yin Guodong¹,Ren Tianbing¹,Rao Yin¹,Zhou Yifan¹,Li Zhexian¹,Shu Wenming²,Wu Anxin²

Affiliation:

1. Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002, PR China

2. Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, Central China Normal University, Wuhan 430079, PR China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo400081q

Reference63 articles.

1. Ueber einige mittelst nascirenden Formaldehydes entstehende Basen

2. New Chiral Molecular Tweezers with a Bis-Tröger's Base Skeleton

3. Molecular clefts. 1. Synthetic methodology for the preparation of analogs of Kagan's ether

4. Synthesis and Self-Aggregation of Enantiopure and Racemic Molecular Tweezers Based on the Bicyclo[3.3.1]nonane Framework

5. Design and Synthesis of a C2-Symmetric Self-Complementary Hydrogen-Bonding Cleft Molecule Based on the Bicyclo[3.3.1]nonane and 4-Oxo-5-azaindole Framework. Formation of Channels and Inclusion Complexes in the Solid State

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