Isolation and structures of -laurencenyne, a possible precursor of the C15 halogenated cyclic ethers, and -neolaurencenyne from-Reference-Cited by-同舟云学术

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Isolation and structures of -laurencenyne, a possible precursor of the C15 halogenated cyclic ethers, and -neolaurencenyne from

Published:1982-01 Issue:14 Volume:23 Page:1475-1476
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kigoshi Hideo,Shizuri Yoshikazu,Niwa Haruki,Yamada Hiyoyuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. - AND -Laurediol, unsaturated glycols from Yamada

2. Laurencenyne, a plausible precursor of various nonterpenoid C15-compounds, and neolaurencenyne from the red alga

3. Laurepinnacin and isolaurepinnacin, new acetylenic cyclic ethers from the marine red alga yamada

4. Conditions: a column of 6 mm × 1.5 m of 10% SILAR 10C, 135 °C, He flow rate 65.5 ml/min.

5. The retention time was 9.2 min. under the conditions employed. 4)

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1. Morphological and Chemical Diversity within Japanese Laurencia Complex (Rhodomelaceae, Ceramiales, Rhodophyta);Chemistry & Biodiversity;2024-09-05

2. Substrate-Controlled Asymmetric Total Synthesis and Structure Revision of (−)-Bisezakyne A;Organic Letters;2016-08-23

3. The Laurencia Paradox: An Endless Source of Chemodiversity;Progress in the Chemistry of Organic Natural Products 102;2016

4. Nonhalogenated organic molecules from Laurencia algae;Phytochemistry Reviews;2013-09-26

5. The stereochemical course of bromoetherification of enynes;Chemical Communications;2008

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