Synthesis and Biological Activity of the C′D′E′F′ Ring System of Maitotoxin

2014 ◽  
Vol 79 (11) ◽  
pp. 4948-4962 ◽  
Author(s):  
Masahiro Kunitake ◽  
Takahiro Oshima ◽  
Keiichi Konoki ◽  
Makoto Ebine ◽  
Kohei Torikai ◽  
...  
2014 ◽  
Vol 18 (03) ◽  
pp. 188-199 ◽  
Author(s):  
Áron Roxin ◽  
Thomas D. MacDonald ◽  
Gang Zheng

Here we show the facile synthesis of 132-173-bacteriochlorophyllone a (12), with a distinct seven-membered exocyclic F-ring formed by 132-173-cyclization of bacteriopheophorbide a(16). This is the latest reported bacteriochlorin with such an exocyclic F-ring since 1975 (132-173 cyclobacteriopheophorbide a-enol, 11), and is an analog of previously described natural exocyclic F-ring-containing porphyrins (1–4) and chlorins (5–10). The structure of 12 was confirmed using a combination of 1D 1 H NMR, 2D COSY 1 H NMR, Jmod 13 C NMR and HRMS analysis. The biological activity of 12 was explored, and we found that this compound does not possess strong antioxidant activity like its natural product counterparts, but is a capable photosensitizer for photodynamic therapy.


1992 ◽  
Vol 152 ◽  
pp. 53-64
Author(s):  
Nicole Borderies

This paper reviews a number of time-dependent phenomena that are relevant to our understanding of the dynamics of planetary rings and that will be investigated using Voyager and Cassini data. A long time baseline may help us decipher the physics of the spokes, understand better the morphology of the F ring and the rigid precession of non-circular ringlets, measure more precisely than has been done so far the satellites' torques and the viscosity of the A ring, and discover small satellites in the Saturnian ring system. Two exciting possibilities are those of determining the recession rates of the small satellites that border the rings, and of observing changes due to viscous diffusion in the irregular structures of the B ring.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1777-C1777
Author(s):  
Hemant Yennawar ◽  
Lee Silverberg ◽  
John Tierney ◽  
Kevin Cannon ◽  
Ryan Bendinsky ◽  
...  

The five-, six-, and seven-membered 1,3-thiaza-4-one heterocycles are known for their bioactivity. Five-membered 1,3-thiazolidin-4-ones are known to have a very wide range of biological activity, so much that the ring system has been referred to as a "magic moiety" or "wonder nucleus" [1]. Six-membered 1,3-thiazin-4-ones have often been investigated for their biological activity and are of potential medicinal use [2]. The activity of seven-membered 1,3-thiazepan-4-ones is exemplified by the investigational compound omapatrilat [3]. Crystal structures of 1,3-thiaza-4-one heterocycles recently obtained in our laboratory will be presented.


ChemInform ◽  
2015 ◽  
Vol 46 (37) ◽  
pp. no-no
Author(s):  
Mohamed A. Waly ◽  
Shiem A. Yossif ◽  
Mamdouh A. Sofan ◽  
Ismail T. Ibrahim

Synlett ◽  
2015 ◽  
Vol 27 (04) ◽  
pp. 621-625 ◽  
Author(s):  
Hidetoshi Tokuyama ◽  
Kosuke Fujioka ◽  
Naoya Miyamoto ◽  
Hiroki Toya ◽  
Kentaro Okano
Keyword(s):  

2008 ◽  
Vol 10 (9) ◽  
pp. 1675-1678 ◽  
Author(s):  
Masayuki Morita ◽  
Seishi Ishiyama ◽  
Hiroyuki Koshino ◽  
Tadashi Nakata

ChemInform ◽  
2010 ◽  
Vol 32 (50) ◽  
pp. no-no
Author(s):  
Yasuharu Sakamoto ◽  
Goh Matsuo ◽  
Hiroko Matsukura ◽  
Tadashi Nakata

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