Synthesis of a Bicyclo[2.2.1]heptane Skeleton with Two Oxy-Functionalized Bridgehead Carbons via the Diels–Alder Reaction
Author:
Affiliation:
1. Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan
2. Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo 060-0810, Japan
Funder
Hokkaido University
Akiyama Life Science Foundation
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c03451
Reference34 articles.
1. Tandem Diels−Alder Cycloadditions in Organic Synthesis
2. Enantioselective Organocatalytic Diels-Alder Reactions
3. Allenes in Diels–Alder Cycloadditions
4. The intramolecular Diels-Alder reaction
5. Harvesting Diels and Alder's Garden: Synthetic Investigations of Intramolecular [4 + 2] Cycloadditions
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