Development of Samarium Diiodide-Promoted Regioselective Carbon-Carbon Bond Cleavage Reaction of γ-Halo- and ε-Halo-α,β-unsaturated Carbonyl Compounds: Application to the Synthesis of Biologically Active Natural Products-Reference-Cited by-同舟云学术

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Development of Samarium Diiodide-Promoted Regioselective Carbon-Carbon Bond Cleavage Reaction of γ-Halo- and ε-Halo-α,β-unsaturated Carbonyl Compounds: Application to the Synthesis of Biologically Active Natural Products

Published:2010 Issue:12 Volume:81 Page:2719
ISSN:0385-5414
Container-title:HETEROCYCLES
language:en
Short-container-title:HETEROCYCLES

Author:

Honda Toshio

Publisher

The Japan Institute of Heterocyclic Chemistry

Subject

Organic Chemistry,Pharmacology,Analytical Chemistry

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Samarium(ii) iodide-mediated reactions applied to natural product total synthesis;RSC Advances;2022

2. The formal synthesis of lucentamycin A: Construction of cis -2,3-disubstituted pyrrolidine core by application of SmI 2 -DMPU system;Tetrahedron Letters;2018-04

3. The formal synthesis of (+)-15-deoxy-Δ12,14-prostaglandin J2: Controlling exo-olefin geometry via SmI2-mediated cyclization;Tetrahedron Letters;2017-10

4. Reversed Electron Apportionment in Mesolytic Cleavage: The Reduction of Benzyl Halides by SmI2;Chemistry - A European Journal;2015-05-12

5. Total Synthesis of Clavilactone B: A Radical Cyclization–Fragmentation Strategy;Organic Letters;2014-12-16

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