ChemInform Abstract: Omaezallene from Red Alga Laurencia sp.: Structure Elucidation, Total Synthesis, and Antifouling Activity.

ChemInform ◽  
2014 ◽  
Vol 45 (36) ◽  
pp. no-no
Author(s):  
Fuyuhiko Matsuda ◽  
et al. et al.
2014 ◽  
Vol 126 (15) ◽  
pp. 3990-3993 ◽  
Author(s):  
Taiki Umezawa ◽  
Yuko Oguri ◽  
Hiroshi Matsuura ◽  
Shohei Yamazaki ◽  
Masahiro Suzuki ◽  
...  

2014 ◽  
Vol 53 (15) ◽  
pp. 3909-3912 ◽  
Author(s):  
Taiki Umezawa ◽  
Yuko Oguri ◽  
Hiroshi Matsuura ◽  
Shohei Yamazaki ◽  
Masahiro Suzuki ◽  
...  

Marine Drugs ◽  
2021 ◽  
Vol 19 (1) ◽  
pp. 35
Author(s):  
Mohamed Shaaban ◽  
Ghada S. E. Abou-El-Wafa ◽  
Christopher Golz ◽  
Hartmut Laatsch

Analysis of the air-dried marine red alga Laurencia papillosa, collected near Ras-Bakr at the Suez gulf (Red Sea) in Egypt delivered five new halogenated terpene derivatives: aplysiolic acid (1), 7-acetyl-aplysiol (2), aplysiol-7-one (3), 11,14-dihydroaplysia-5,11,14,15-tetrol (5a), and a new maneonene derivative 6, named 5-epi-maneolactone. The chemical structures of these metabolites were characterized employing spectroscopic methods, and the relative and absolute configurations were determined by comparison of experimental and ab initio-calculated NMR, NOE, ECD, and ORD data, and by X-ray diffraction of 2 and 6. The antimicrobial activities of the crude extract and compounds 1–3, 5a and 6 were studied.


ChemInform ◽  
2015 ◽  
Vol 46 (22) ◽  
pp. no-no
Author(s):  
Eiji Nishimura ◽  
Yasufumi Ohfune ◽  
Tetsuro Shinada

Synlett ◽  
2020 ◽  
Vol 32 (01) ◽  
pp. 45-50
Author(s):  
Udo Nubbemeyer ◽  
Analuisa Nava ◽  
Lukas Trippe ◽  
Andrea Frank ◽  
Lars Andernach ◽  
...  

AbstractStarting from methyl cycloheptatrienyl-1-carboxylate, 6-acylation was successfully achieved employing glutaryl chloride in the presence of AlCl3 under controlled reaction conditions to furnish keto carboxylic acid product. After protection of this keto carboxylic acid as tert-butyl ester, reagent-controlled enantioselective reductions delivered configuration-defined methyl-6-hydroxylalkyl cycloheptatriene-1-carboxylates with up to 80% ee. Whereas simple NaBH4 reduction of the keto carboxylic acid and subsequent lactonization afforded a methyl-6-tetrahydropyranonyl cycloheptatriene-1-carboxylate. Resolution using chiral HPLC delivered the product enantiomers with up to >99% ee Finally, ECD analyses enabled structure elucidation. The products are used as key intermediates in enantioselective 6,11-methylene-lipoxin B4 syntheses.


2011 ◽  
Vol 123 (12) ◽  
pp. 2768-2771 ◽  
Author(s):  
Klement Foo ◽  
Timothy Newhouse ◽  
Ikue Mori ◽  
Hiromitsu Takayama ◽  
Phil S. Baran

2014 ◽  
Vol 53 (7) ◽  
pp. 1795-1798 ◽  
Author(s):  
Gerrit Symkenberg ◽  
Markus Kalesse

2010 ◽  
Vol 8 (9) ◽  
pp. 2123 ◽  
Author(s):  
Katharina Götz ◽  
Johannes C. Liermann ◽  
Eckhard Thines ◽  
Heidrun Anke ◽  
Till Opatz

2009 ◽  
Vol 131 (4) ◽  
pp. 1392-1393 ◽  
Author(s):  
Todd K. Macklin ◽  
Glenn C. Micalizio

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