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Dual Rh(II)/Pd(0) Relay Catalysis Involving Sigmatropic Rearrangement Using N-Sulfonyl Triazoles and 2-Hydroxymethylallyl Carbonates

Authors
Huang, Liang-ZhuXuan, ZiPark, Jong-UnKim, Ju Hyun
Issue Date
Sep-2022
Publisher
AMER CHEMICAL SOC
Citation
ORGANIC LETTERS, v.24, no.38, pp.6951 - 6956
Indexed
SCIE
SCOPUS
Journal Title
ORGANIC LETTERS
Volume
24
Number
38
Start Page
6951
End Page
6956
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/2804
DOI
10.1021/acs.orglett.2c02752
ISSN
1523-7060
Abstract
Dual Rh(II)/Pd(0) relay catalysis of N-sulfonyl triazoles and 2-hydroxymethylallyl carbonates has been developed, which affords N-sulfonyl pyrrolidines in moderate to good yields with high diastereoselectivities. The reaction proceeds via a relay mechanism involving O-H insertion onto the alpha-imino Rh(II)-carbene, [3,3]-sigmatropic rearrangement, dipole formation through Pd(0)-catalyzed decarboxylation, and intramolecular N-allylation, leading to the formation of multiple bonds in a one-pot operation.
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