Stereoselectivity in a nitroso-ene cyclization: Formal synthesis of rac-manzacidins A and C-Reference-Cited by-同舟云学术

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Stereoselectivity in a nitroso-ene cyclization: Formal synthesis of rac-manzacidins A and C

Published:2019-03 Issue:12 Volume:75 Page:1767-1773
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Liu Ying,Ruan Zhuwei,Wang Yan,Huang Sha-Hua,Hong Ran

Funder

Innovation Program of Shanghai Institute of Technology

National Natural Science Foundation of China

Shanghai Sailing Program

Shanghai Municipal Science and Technology Commission

Chinese Academy of Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. A rationalization of nitrosoarene-olefin reactions

2. Tilden Lecture. Electrophilic C-nitroso-compounds

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1. Core Structure-Oriented Asymmetric α-Allenylic Alkylation of Amino Acid Esters Enabled by Chiral Aldehyde/Palladium Catalysis;Organic Letters;2023-12-22

2. Total Synthesis of Immunosuppressive Mycestericin E and G Enabled by a Highly Stereoselective Nitroso–Ene Cyclization;Organic Letters;2023-05-08

3. Nitroso-Ene-type Cyclization Toward Diversified Synthesis of Amino Deoxysugars: A Proof of Concept;Organic Letters;2023-03-13

4. Aza-Wacker Cyclization Toward the Bridged Core of FR901483;Synthesis;2023-01-13

5. Aerobic C−N Bond Formation through Enzymatic Nitroso‐Ene‐Type Reactions**;Angewandte Chemie International Edition;2023-01-09

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