New cadinane sesquiterpenoids from the basidiomycetous fungus Pholiota sp.

RSC Advances ◽  
2016 ◽  
Vol 6 (113) ◽  
pp. 112527-112533 ◽  
Author(s):  
Jie Lin ◽  
Renlei Wang ◽  
Guohua Xu ◽  
Zhengfeng Ding ◽  
Xueshen Zhu ◽  
...  

The basidiomycetous fungus Pholiota sp. produced five new cadinane sesquiterpenoids pholiotins A–E (1–5). The absolute configurations were determined by X-ray diffraction, the Snatzke's method and electronic circular dichroism (ECD) calculations.

Author(s):  
Danyang Zhang ◽  
Xiao-Xia Wang ◽  
Ya-Nan Wang ◽  
Min Wang ◽  
Peng-Yu Zhuang ◽  
...  

Chlorahupetones A-I (1−9), nine sesquiterpenoid dimers, were isolated from Chloranthus henryi var. hupehensis. Their structures were characterized by nuclear magnetic resonance (NMR), electronic circular dichroism (ECD), and X-ray diffraction analysis....


RSC Advances ◽  
2016 ◽  
Vol 6 (85) ◽  
pp. 81461-81465 ◽  
Author(s):  
M. Kohout ◽  
J. Vandenbussche ◽  
A. Roller ◽  
J. Tůma ◽  
J. Bogaerts ◽  
...  

The long-standing discussion of the absolute configuration of erythro-mefloquine is revisited, showcasing the strength of a combination of experimental and calculated vibrational circular dichroism spectroscopy.


2017 ◽  
Vol 46 (13) ◽  
pp. 4397-4402 ◽  
Author(s):  
Kazuyoshi Takimoto ◽  
Yutaka Watanabe ◽  
Shigeki Mori ◽  
Hisako Sato

The absolute configuration of a cationic iridium(iii) complex was determined in solution and solid by vibrational circular dichroism and X-ray diffraction analyses.


1983 ◽  
Vol 36 (5) ◽  
pp. 1037 ◽  
Author(s):  
IRC Bick ◽  
MA Hai ◽  
VA Patrick ◽  
AH White

The crystal structure of the alkaloid aristoserratine,* C20H24N2O, has been determined by single-crystal X-ray diffraction methods at 295 K, the structure being refined to a residual of 0.034 for 1107 independent 'observed' reflections. Crystals are monoclinic, P21, a 14.836(5), b 8.568(3), c 6.633(3) �, β 98.05(3)�, Z 2. The relative configuration is established and, by inference, by comparison of the circular dichroism spectrum with that of aristoteline, the absolute configuration is assigned.


Chemosensors ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 154
Author(s):  
Stefania Vergura ◽  
Stefano Orlando ◽  
Patrizia Scafato ◽  
Sandra Belviso ◽  
Stefano Superchi

The absolute configuration of chiral 2-aryl and 2-aryloxy propionic acids, which are among the most common chiral environmental pollutants, has been readily and reliably established by either electronic circular dichroism spectroscopy or optical rotation measurements employing suitably designed 4,4′-disubstituted biphenyl probes. In fact, the 4,4′-biphenyl substitution gives rise to a red shift of the diagnostic electronic circular dichroism signal of the biphenyl A band employed for the configuration assignment, removing its overlap with other interfering dichroic bands and allowing its clear sign identification. The largest A band red shift, and thus the most reliable results, are obtained by employing as a probe the 4,4′-dinitro substituted biphenylazepine 3c. The method was applied to the absolute configuration assignment of 2-arylpropionic acids ibuprofen (1a), naproxen (1b), ketoprofen (1c) and flurbiprofen (1d), as well as to the 2-aryloxypropionic acids 2-phenoxypropionic acid (2a) and 2-naphthoxypropionic acid (2b). This approach, allowing us to reveal the sample’s absolute configuration by simple optical rotation measurements, is potentially applicable to online analyses of both the enantiomeric composition and absolute configuration of these chiral pollutants.


2011 ◽  
Vol 22 (6) ◽  
pp. 1241-1248 ◽  
Author(s):  
Xiao-Bing Wang ◽  
Yao Zhang ◽  
Jun-Song Wang ◽  
He-Quan Yao ◽  
Hong-Bin Sun ◽  
...  

2004 ◽  
Vol 345 (1-4) ◽  
pp. 213-216 ◽  
Author(s):  
Ming-Zhe Lin ◽  
Chih-Hao Lee ◽  
Kuan-Li Yu ◽  
J.C.A. Huang ◽  
W.C. Chen

Sign in / Sign up

Export Citation Format

Share Document