Enantioselective Michael Addition/Cyclization/Desymmetrization Sequence of Prochiral Cyclic Hemiacetals and Nitroolefins: Synthesis of Chiral Oxygen-Bridged Bicyclic Compounds-Reference-Cited by-同舟云学术

Enantioselective Michael Addition/Cyclization/Desymmetrization Sequence of Prochiral Cyclic Hemiacetals and Nitroolefins: Synthesis of Chiral Oxygen-Bridged Bicyclic Compounds

Published:2022-12-13 Issue:50 Volume:24 Page:9254-9258
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Yu-Jie¹,Lv Xue-Jiao¹,Liu Yan-Kai¹²^ORCID

Affiliation:

1. Molecular Synthesis Center & Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China

2. Laboratory for Marine Drugs and Bioproducts of Qingdao National Laboratory for Marine Science and Technology, Qingdao 266003, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03815

Reference38 articles.

1. Diastereoselective Synthesis of Seven- and Eight-Membered Oxabicycles via Prins-Type Cyclization

2. Substituted 9-Oxabicyclo[4.2.1]- and 9-Oxabicyclo[3.3.1]nonanes (Part II)

3. Total syntheses of (+)-nogarene and (+)-7,8-dihydronogarene

4. On the Origin of Siphonariid Polypropionates: Total Synthesis of Caloundrin B and Its Isomerization to Siphonarin B

5. Synthetic studies on nogalamycin congeners [1]1 chiral synthesis of the def-ring system of nogalamycin

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