Tunable Reaction Mode of Bifunctional Peroxides with Ketones to Access α-Oxacyclic Ketones and Enals-Reference-Cited by-同舟云学术

Tunable Reaction Mode of Bifunctional Peroxides with Ketones to Access α-Oxacyclic Ketones and Enals

Published:2022-11-09 Issue:45 Volume:24 Page:8387-8391
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wen Xiaolu¹,Gao Min²,Chen Yiwei¹,Zhao Yukun¹,Qin Wenling¹^ORCID,Hu Lin¹^ORCID

Affiliation:

1. Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China

2. College of Chemistry and Chemical Engineering, Yan’an University, Yan’an 716000, China

Funder

Natural Science Foundation of Chongqing

Central University Basic Research Fund of China

National Natural Science Foundation of China

Venture & Innovation Support Program for Chongqing Overseas Returnees

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03440

Reference40 articles.

1. A Short Total Synthesis of (+)-Furanomycin

2. Synthesis and olfactory evaluation of the enantiomerically enriched forms of 7,11-epoxymegastigma-5(6)-en-9-one and 7,11-epoxymegastigma-5(6)-en-9-ols isomers, identified in Passiflora edulis

3. Total Synthesis of Antascomicin B

4. Synthesis of cis- and trans-Davanoids: Artemone, Hydroxydavanone, Isodavanone, and Nordavanone

5. Total Synthesis of (−)-Luminacin D

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