Epoxy lactones by photooxidative rearrangement of 6β-acetoxyvouacapane-Reference-Cited by-同舟云学术

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Epoxy lactones by photooxidative rearrangement of 6β-acetoxyvouacapane

Published:2017-07 Issue:30 Volume:58 Page:2901-2903
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Talavera-Alemán Armando,Gómez-Hurtado Mario A.,Río Rosa E. del,Marrot Jérôme,Thomassigny Christine,Greck Christine

Funder

CIC

UMSNH

CONACYT

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Using Singlet Oxygen to Synthesize Polyoxygenated Natural Products from Furans

2. γ-Spiroketal γ-Lactones from 2-(γ-Hydroxyalkyl)furans: Syntheses of epi-Pyrenolides D and Crassalactone D

3. Scope and Limitations of the Photooxidations of 2-(α-Hydroxyalkyl)furans: Synthesis of 2-Hydroxy-exo-brevicomin

4. Oxidation of furans (Review)

5. Photo-oxidation of furans

Cited by 4 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. Late‐stage functionalization of Vouacapane derivatives from Caesalpinia platyloba by a Groebke−Blackburn−Bienaymé reaction;Journal of Heterocyclic Chemistry;2023-07-15

2. Visible light-mediated applications of methylene blue in organic synthesis;Organic Chemistry Frontiers;2021

3. Preparation and Cytotoxic Evaluation of Vouacapane Oxidation Products;HETEROCYCLES;2020

4. Diterpenoids of terrestrial origin;Natural Product Reports;2019

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