Sequential Diels–Alder Reaction/Rearrangement Sequence: Synthesis of Functionalized Bicyclo[2.2.1]heptane Derivatives and Revision of Their Relative Configuration-Reference-Cited by-同舟云学术

Sequential Diels–Alder Reaction/Rearrangement Sequence: Synthesis of Functionalized Bicyclo[2.2.1]heptane Derivatives and Revision of Their Relative Configuration

Published:2014-06-30 Issue:14 Volume:79 Page:6726-6731
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liang Demin¹,Zou Yue²,Wang Quanrui¹,Goeke Andreas²

Affiliation:

1. Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, People’s Republic of China

2. Givaudan Fragrances (Shanghai) Ltd, Li Shi Zhen Road 298, Shanghai 201203, People’s Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500942a

Reference23 articles.

1. Tandem Diels−Alder Cycloadditions in Organic Synthesis

2. Tandem Diels−Alder/Ene Reactions

3. Lewis Acid Promoted Tandem Intermolecular Diels−Alder/Intramolecular Allylation Reactions of Silyl-Substituted 1,3-Butadienes Leading to Multisubstituted 7-Norbornenones and Related Polycyclic Compounds

4. Lewis Acid Induced Tandem Diels−Alder Reaction/Ring Expansion as an Equivalent of a [4 + 3] Cycloaddition

5. Formal Enantioselective [4+3] Cycloaddition by a Tandem Diels–Alder Reaction/Ring Expansion

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