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Three new vinyl acetylenes from the marine red alga laurencia

✍ Scribed by Bruce M. Howard; Gary R. Schulte; William Fenical; Barbara Solheim; Jon Clardy


Book ID
107857098
Publisher
Elsevier Science
Year
1980
Tongue
French
Weight
415 KB
Volume
36
Category
Article
ISSN
0040-4020

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πŸ“œ SIMILAR VOLUMES


Laurencienyne, a new acetylenic cyclic e
✍ Salvatore Caccamese; Roberto Azzolina; Eileen N. Duesler; Iain C. Paul; Kenneth πŸ“‚ Article πŸ“… 1980 πŸ› Elsevier Science 🌐 French βš– 201 KB

The structure and absolute stereochemistry of laurencienyne, a non-isoprenoid cyclic ether isolated from Laurencia obtusa, has been established by X-ray and spectroscopic studies. In our continuing effort to screen marine algae from Eastern Sicily for antimicrobial activity and to isolate the active

Sesquiterpenes from the Marine Red Alga
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## Abstract Together with five known sesquiterpenes, EtOH extraction of __Laurencia saitoi__ yielded four new compounds, including three sesquiterpenes and one norsesquiterpene derivative. Their structures and relative configurations were elucidated by spectroscopic methods, including 1D‐ and 2D‐NM