Development of radical addition–cyclization–elimination reaction of oxime ether and its application to formal synthesis of (±)-martinelline-Reference-Cited by-同舟云学术

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Development of radical addition–cyclization–elimination reaction of oxime ether and its application to formal synthesis of (±)-martinelline

Published:2007-10 Issue:40 Volume:63 Page:10092-10117
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Miyata Okiko,Shirai Atsushi,Yoshino Shintaro,Nakabayashi Toshiki,Takeda Yoshifumi,Kiguchi Toshiko,Fukumoto Daisuke,Ueda Masafumi,Naito Takeaki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference93 articles.

1. Domino Reactions in Organic Synthesis;Tietze,2006

2. Radical cyclisation in heterocycle synthesis. Part 1. Sulfanyl radical addition–cyclisation of dienylamides for lactam synthesis

3. Hydroximate as a synthetically useful functional group: A novel synthesis of lactones using hydroximates as a tether

4. HYDROXIMATE AS A SYNTHETICALLY USEFUL FUNCTIONAL GROUP Part II : SYNTHESIS OF (±)-OXO-PARABENZLACTONE

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1. Study of the Mechanism of 7‐exo‐trig Cyclizations of Aryl, Vinyl, and Alkyl Radicals on Oxime Ethers;European Journal of Organic Chemistry;2024-01-19

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3. Multicomponent Reactions in Natural Product Synthesis;Efficiency in Natural Product Total Synthesis;2018-08-06

4. Iridium(III)-Catalyzed Directed ortho -C(sp2 )-H Amidation of Arenes with Sulfonamides;European Journal of Organic Chemistry;2018-05-08

5. Catalytic Enantioselective Synthesis of the Partially Reduced Tricyclic Pyrrolo[3,2-c]quinoline Core Structure of theMartinellaAlkaloids;ChemistrySelect;2016-06-01

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