Tandem Double-Intramolecular [4+2]/[3+2] Cycloadditions of Nitroalkenes. Studies toward a Total Synthesis of Daphnilactone B: Piperidine Ring Construction-Reference-Cited by-同舟云学术

Tandem Double-Intramolecular [4+2]/[3+2] Cycloadditions of Nitroalkenes. Studies toward a Total Synthesis of Daphnilactone B: Piperidine Ring Construction

Published:2005-12-17 Issue:2 Volume:71 Page:593-605
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Denmark Scott E.¹,Baiazitov Ramil Y.¹

Affiliation:

1. Department of Chemistry, Roger Adams Laboratory, University of Illinois, Urbana, Illinois 61801

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo052001l

Reference56 articles.

1. (a) Denmark, S. E.; Cottell, J. J. InThe Chemistry of HeterocyclicCompounds: Synthetic Applications of 1,3-Dipolar Cycloaddition ChemistryToward Heterocycles and Natural Products; Padwa, A., Pearson, W. H., Eds.; Wiley-Interscience: New York, 2002; pp 83−167.

2. Tandem [4+2]/[3+2] Cycloadditions of Nitroalkenes

3. Studies on the reduction and hydrolysis of nitroso acetals

Cited by 88 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pd‐Catalyzed Chemoselective Bis‐Allylic Substitution of Allylic Dicarbonates with Arylated Nitromethanes: A Route to 1,2‐Oxazine N ‐Oxides;Asian Journal of Organic Chemistry;2022-03-16

2. Mechanistic studies on stereoselective domino [4 + 2]/retro[3 + 2]/[3 + 2] cycloaddition reactions of oxadiazoles with strained and unstrained cycloalkenes;Theoretical Chemistry Accounts;2022-02

3. New Secodaphnane-Type Alkaloids with Cytotoxic Activities from Daphniphyllum angustifolium Hutch;Natural Products and Bioprospecting;2021-05-11

4. Visible Light-Induced Pericyclic Cascade Reaction for the Synthesis of Quinolinone Derivatives with an Oxabicyclo[4.2.0]octene Skeleton;Organic Letters;2021-03-30

5. The chemistry of Daphniphyllum alkaloids;The Alkaloids: Chemistry and Biology;2021