Synthesis of Enantioenriched γ-Amino-α,β-unsaturated Esters Utilizing Palladium-Catalyzed Rearrangement of Allylic Carbamates for Direct Application to Formal [3 + 2] Cycloaddition-Reference-Cited by-同舟云学术

Synthesis of Enantioenriched γ-Amino-α,β-unsaturated Esters Utilizing Palladium-Catalyzed Rearrangement of Allylic Carbamates for Direct Application to Formal [3 + 2] Cycloaddition

Published:2017-03-17 Issue:7 Volume:19 Page:1682-1685
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kondoh Azusa¹^ORCID,Kamata Yuji¹,Terada Masahiro¹^ORCID

Affiliation:

1. Research and Analytical Center for Giant Molecules, Graduate School of Science and ‡Department of Chemistry, Graduate School of Science, Tohoku University, Aoba-ku, Sendai 980-8578, Japan

Funder

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.7b00471

Reference27 articles.

1. Thermal rearrangement of allylic phenylurethanes

2. Decarboxylative cyclization of allylic cyclic carbamates: applications to the total synthesis of (-)-codonopsine

3. A Facile Highly Regio- and Stereoselective Preparation of N-Tosyl Allylic Amines from Allylic Alcohols and Tosyl Isocyanate via Palladium(II)-Catalyzed Aminopalladation−β-Heteroatom Elimination