Synthesis of (+)-laurencin via ring expansion of a C-glycoside derivative-Reference-Cited by-同舟云学术

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Synthesis of (+)-laurencin via ring expansion of a C-glycoside derivative

Published:2005-10 Issue:40 Volume:46 Page:6819-6822
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujiwara Kenshu,Yoshimoto Saori,Takizawa Ayumi,Souma Shin-ichiro,Mishima Hirofumi,Murai Akio,Kawai Hidetoshi,Suzuki Takanori

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference48 articles.

1. A new vinyl acetylene from the red alga Laurencia thyrsifera

2. Metabolites of the marine red alga Laurencia thyrsifera. III

3. A new synthetic method for the preparation of 2,8-disubstituted oxocane derivatives: synthesis of lauthisan and laurenan

4. Isomerization of the (Z)-Enyne Unit to the (E)-Enyne Unit. Conversion of Laureatin to (E)-Isolaureatin

5. Laurencin, a constituent from species

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1. Synthesis of diazocines and oxocines by cyclization of dienes;8-Membered Heterocycle Synthesis;2023

2. Forwards and backwards – synthesis of Laurencia natural products using a biomimetic and retrobiomimetic strategy incorporating structural reassignment of laurefurenynes C–F;Chemical Science;2020

3. General Synthetic Approach for the Laurencia Family of Natural Products Empowered by a Potentially Biomimetic Ring Expansion;Journal of the American Chemical Society;2019-04-16

4. Asymmetric synthesis of (+)-laurencin using a stereoselective Stevens [1,2]-shift of a sulfonium ylide;Strategies and Tactics in Organic Synthesis;2019

5. Formal Synthesis of (+)‐Laurencin by Gold(I)‐Catalyzed Intramolecular Dehydrative Alkoxylation;Chemistry – A European Journal;2017-05-03

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