Stereoselective Synthesis of Conjugated Di- and Trienamides via a Dienolate Enabled Anionic Cascade-Reference-Cited by-同舟云学术

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Stereoselective Synthesis of Conjugated Di- and Trienamides via a Dienolate Enabled Anionic Cascade

Published:2023-12-04 Issue:24 Volume:88 Page:17485-17488
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bao Jianhua¹,Nick Steven J.¹,Lanin Aleksey S.¹,Iragorri Molinero Nerea¹,Sera Brendon J.¹,Njardarson Jon T.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona 85721, United States

Funder

Division of Chemistry

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02327

Reference18 articles.

1. Charge-accelerated cope rearrangements of 3-amino-1,5-dienes

2. The first example of asymmetric induction in an anionic amino-Cope rearrangement

3. New Paradigm for Anionic Heteroatom Cope Rearrangements

4. [1,3] and [3,3] rearrangements of 3-amino-1,5-hexadienes: Solvent effect on the regioselectivity

5. Evidence for alternative mechanisms in the amino-Cope rearrangement

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1. Masters of Mediation: MN(SiMe₃)₂ in Functionalization of C(sp³)−H Latent Nucleophiles;Chemistry – A European Journal;2024-04-16

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