scholarly journals Diacetyl-atractylodiol, a new acetylenic compound from Atractylodes japonica KOIDZUMI.

1974 ◽  
Vol 22 (8) ◽  
pp. 1943-1945 ◽  
Author(s):  
ITIRO YOSIOKA ◽  
TADATO TANI ◽  
MIHOKO HIROSE ◽  
ISAO KITAGAWA
Keyword(s):  
Acetylenic Compound ◽  
Atractylodes Japonica

scholarly journals The complete chloroplast genome of Atractylodes japonica Koidz. ex Kitam. and its phylogenetic inference

2021 ◽  
Vol 6 (7) ◽  
pp. 2038-2040
Author(s):  
Mengmeng Shi ◽  
Hongbo Xie ◽  
Chunying Zhao ◽  
Linchun Shi ◽  
Jinxin Liu ◽  
...  
Keyword(s):  
Chloroplast Genome ◽  
Phylogenetic Inference ◽  
Complete Chloroplast Genome ◽  
Atractylodes Japonica

Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi

2016 ◽  
Vol 64 (11) ◽  
pp. 2254-2262 ◽  
Author(s):  
Lih-Geeng Chen ◽  
Yun-Sheng Jan ◽  
Po-Wei Tsai ◽  
Hisayoshi Norimoto ◽  
Seiwa Michihara ◽  
...  
Keyword(s):  
Atractylodes Japonica ◽  
Anti Inflammatory

ChemInform Abstract: AN UNUSUAL TRANSANNULAR REACTION IN AN EIGHT-ATOM RING DURING HYDRATION OF AN ACETYLENIC COMPOUND

1977 ◽  
Vol 8 (43) ◽  
pp. no-no
Author(s):  
R. BALASUBRAMANIAN ◽  
K. RAJAGOPALAN ◽  
K. G. SRINIVASAN ◽  
S. SWAMINATHAN
Keyword(s):  
Acetylenic Compound ◽  
Transannular Reaction

scholarly journals Development of 18 microsatellite markers for Atractylodes japonica

2020 ◽  
Vol 8 (5) ◽  
Author(s):  
Jin‐Tae Jeong ◽  
Hee Chung ◽  
Bo‐Keun Ha ◽  
Jinsu Gil ◽  
Jeong‐Hoon Lee ◽  
...  
Keyword(s):  
Microsatellite Markers ◽  
Atractylodes Japonica

Chemical Structure-Odor Correlation in a Series of Synthetic n-Nonen-1-ols

1995 ◽  
Vol 50 (11-12) ◽  
pp. 757-765 ◽  
Author(s):  
Yasunobu Sakoda ◽  
Kenji Matsui ◽  
Tadahiko Kajiwara ◽  
Akikazu Hatanaka
Keyword(s):  
Principal Component Analysis ◽  
Double Bond ◽  
Spatial Structure ◽  
Chemical Structure ◽  
Principal Component ◽  
Component Analysis ◽  
Acetylenic Compound ◽  
Analysis Method ◽  
Entire Series ◽  
Novel Method

In order to elucidate chemical structure-odor correlation in the all isomers of n-nonen-1- ols, an entire series of these alcohols were synthesized stereo-selectively in high purity. For unequivocal syntheses of them, geometrically selective hydrogenation of the respective acetylenic compound was adopted. The synthesized alcohols were converted to their 3,5-dinitrobenzoate derivatives with 3,5-dinitrobenzoyl chloride, and then purified by repeated recrystallization. Chemical structure-odor correlations in all the isomers of n-nonen-1-ols were elucidated by introducing a novel method to evaluate odor characteristics and by treating the obtained data statistically with the principal component analysis method (Cramer et al., 1988). The odor profiles of the tested compounds were attributable largely to the positions of the carbon- double bond. The geometries of compounds had only a little effect. With the principal component analysis, the odor profiles of the series of compounds were successfully integrated into the first and the second principal components. The first component (PC-1) consisted of combined characteristics of fruity, fresh, sweet, herbal and oily-fatty, in which herbal and oily-fatty were conversely correlated each other to the position of double-bond of the tested compounds. Of these, only (6Z)-nonen-1-ol deviated markedly from the correlation, indicative of some special interaction between the spatial structure of this compound and the sensory machinery of human.

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