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1. Enantiomeric distribution of odour-active epoxyaldehydes in yuzu (Citrus junos Sieb. ex Tanaka)
by Miyazato, Hironari and Hashimoto, Seiji and Hayashi, Shuichi
European Food Research and Technology, ISSN 1438-2377, 12/2013, Volume 237, Issue 6, pp. 933 - 942
The odour-active epoxyaldehydes cis-4,5-epoxy-(E)-2-decenal (1), trans-4,5-epoxy-(E)-2-decenal (2), and trans-4,5-epoxy-(E,Z)-2,7-decadienal (3) are present in... 
Absolute configuration
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2. Full Text Determination of the Absolute Configuration of (−)‐Hydroxynitrilaphos and Related Biosynthetic Questions
by Pallitsch, Katharina and Happl, Barbara and Stieger, Christian
Chemistry – A European Journal, ISSN 0947-6539, 11/2017, Volume 23, Issue 62, pp. 15542 - 15542
Invited for the cover of this issue is the group of Katharina Pallitsch at the University of Vienna. The image depicts an rendition of the still unknown... 
Biosynthesis | Enzymology | Metabolism | Absolute configuration
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3. Stereocontrolled synthesis of oligonucleotide analogs containing chiral internucleotidic phosphorus atoms
by Oka, Natsuhisa and Wada, Takeshi
Chemical Society Reviews, ISSN 0306-0012, 01/2011, Volume 40, Issue 12, pp. 5829 - 5843
Oligonucleotides, in which one of the two nonbridging oxygen atoms of internucleotidic phosphates is replaced by a different type of atom or a substituent, are... 
Absolute configuration
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4. Full Text Evolvulins I and II, Resin Glycosides with a Trihydroxy Aglycone Unit from Evolvulus alsinoides
by Fan, BY and Lu, Y and Yang, M and Li, JL and Chen, GT
ORGANIC LETTERS, ISSN 1523-7060, 08/2019, Volume 21, Issue 16, pp. 6548 - 6551
Evolvulins I and II (1 and 2), representing a new class of resin glycosides with an unprecedented trihydroxy aglycone unit, 3S,11R,14R-trihydroxyhexadecanoic... 
ABSOLUTE-CONFIGURATION | CHEMISTRY, ORGANIC
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5. Full Text Single-crystal structure validation with the program PLATON
by Spek, A.L.|info:eu-repo/dai/nl/156517566
Journal of Applied Crystallography, ISSN 0021-8898, 2003, Volume 36, Issue 1, pp. 7 - 13
The results of a single‐crystal structure determination when in CIF format can now be validated routinely by automatic procedures. In this way, many errors in... 
data validation | crystallographic information file (CIF) | ABSOLUTE-CONFIGURATION | CRYSTALLOGRAPHY | SYMMETRY
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6. Full Text Crystal structure of 5,4′-dihydroxy-7,3′-dimethoxyflavanone, C17H16O6
by Cisterna, Jonathan and Bórquez, Jorge and Muñoz, Rubén and Simirgiotis, Mario and Cárdenas, Alejandro and Brito, Iván
Zeitschrift für Kristallographie - New Crystal Structures, ISSN 1433-7266, 03/2019, Volume 234, Issue 3, pp. 405 - 407
, orthorhombic, (no. 19), = 5.2601(3) Å, = 12.7161(6) Å, = 22.0116(11) Å, = 1472.31(13) Å , = 4, ) = 0.0430, ) = 0.1089, = 296(2) K. 
1889566 | ABSOLUTE-CONFIGURATION | DITERPENOIDS | CRYSTALLOGRAPHY
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7. Full Text Enantiodiscrimination by matrix-assisted DOSY NMR
by Salome, KS and Tormena, CF
CHEMICAL COMMUNICATIONS, ISSN 1359-7345, 07/2019, Volume 55, Issue 59, pp. 8611 - 8614
High-resolution NMR is an essential technique for structure determination; however, stereochemistry assignment is still an obstacle. Several methods are known... 
F-19 NMR | ABSOLUTE-CONFIGURATION | DISCRIMINATION | VERSATILE | CHEMISTRY, MULTIDISCIPLINARY
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8. Full Text Polycyclic furanobutenolide-derived norditerpenoids from the South China Sea soft corals Sinularia scabra and Sinularia polydactyla with immunosuppressive activity
by Cui, Wan-Xiang and Yang, Min and Li, Heng and Li, Song-Wei and Yao, Li-Gong and Li, Geng and Tang, Wei and Wang, Chun-Hua and Liang, Lin-Fu and Guo, Yue-Wei
Bioorganic Chemistry, ISSN 0045-2068, 10/2019, p. 103350
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9. Full Text Experimental and theoretical study of stereochemistry for new pseurotin A3with an unusual hetero-spirocyclic system
by Xu, Lan-Lan and Cao, Fei and Yang, Qin and Li, Wan and Tian, Sha-Sha and Zhu, Hua-Jie and Zhao, Yan-Yan and Yang, Xun
Tetrahedron, ISSN 0040-4020, 2016, Volume 72, Issue 45, pp. 7194 - 7199
A new pseurotin A (3), which was obtained from the fungus Aspergillus terreus was converted into its acetyl derivative (4). Optical rotation (OR), C NMR,... 
Chiroptical spectroscopies | Absolute configuration | C NMR | Pseurotin A
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10. Full Text Cyclombandakamines A(1) and A(2), Oxygen-Bridged Naphthylisoquinoline Dimers from a Congolese Ancistrocladus Liana
by Lombe, BK and Bruhn, T and Feineis, D and Mudogo, V and Brun, R and Bringrnann, G
ORGANIC LETTERS, ISSN 1523-7060, 03/2017, Volume 19, Issue 6, pp. 1342 - 1345
Cyclombandakamines A(1) (I) and A(2) (2), both with an unprecedented pyrane cyclohexenone dihydrofuran sequence and six stereocenters and two chiral axes, are... 
DIONCOPHYLLACEAE | ABSOLUTE-CONFIGURATION | ISOQUINOLINE | GENUS | CHEMISTRY, ORGANIC | AXES | ALKALOIDS
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11. Full Text Flueggeacosines A–C, Dimeric Securinine-Type Alkaloid Analogues with Neuronal Differentiation Activity from Flueggea suffruticosa
by Wu, Zhen-Long and Huang, Xiao-Jun and Xu, Ming-Tao and Ma, Xuanyue and Li, Liuren and Shi, Lei and Wang, Wen-Jing and Jiang, Ren-Wang and Ye, Wen-Cai and Wang, Ying
Organic Letters, ISSN 1523-7060, 12/2018, Volume 20, Issue 23, pp. 7703 - 7707
Flueggeacosines A–C (1–3), three dimeric securinine-type alkaloid analogues with unprecedented skeletons, were isolated from Flueggea suffruticosa. Compounds 1... 
CHEMISTRY, ORGANIC | ABSOLUTE-CONFIGURATION | INDOLIZIDINE ALKALOIDS | SKELETON
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12. Full Text Synthesis and Photochemical Properties of Axially Chiral Bis(dinaphthofuran)
by Katakami, Chiaki and Kamo, Shogo and Torii, Ayame and Hara, Nobuyuki and Imai, Yoshitane and Taniguchi, Tohru and Monde, Kenji and Okabayashi, Yusuke and Hosokai, Takuya and Kuramochi, Kouji and Tsubaki, Kazunori
The Journal of Organic Chemistry, ISSN 0022-3263, 12/2018, Volume 83, Issue 23, pp. 14610 - 14616
Both enantiomers of axially chiral bis­(dinaphthofuran) were prepared in only two steps from 1′-hydroxy-4′-methoxy-2,2′-binaphthalenyl-1,4-dione, followed by... 
CIRCULARLY-POLARIZED LUMINESCENCE | CHEMISTRY, ORGANIC | ABSOLUTE-CONFIGURATION | FLUORESCENCE | ALGORITHM
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13. Full Text Cover Feature: Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes (Chem. Eur. J. 22/2019)
by Vergura, Stefania and Scafato, Patrizia and Belviso, Sandra and Superchi, Stefano
Chemistry – A European Journal, ISSN 0947-6539, 04/2019, Volume 25, Issue 22, pp. 5597 - 5597
A central‐to‐axial chirality transfer occurring when chiral molecules are linked to flexible biphenyl probes makes it possible to assign their absolute... 
biphenyls | chiroptical probes | circular dichroism | absolute configuration | optical rotation
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14. A new [alpha]-pyrone from the deep-sea actinomycete Nocardiopsis dassonvillei subsp. dassonvillei DSM 43111(T)
by Ge Zou and Xiao-Jian Liao and Qi Peng and Guo-Dong Chen and Fang-Ying Wei and Zheng-Xiong Xu and Bing-Xin Zhao and Shi-Hai Xu
Journal of Asian Natural Products Research, ISSN 1028-6020, 12/2017, Volume 19, Issue 12, p. 1232
A new α-pyrone, nocapyrone S (1), together with five known compounds (2-6), were isolated from the deep-sea actinomycete Nocardiopsis dassonvillei subsp.... 
Absolute configuration | Cell lines | Cytotoxicity
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15. Full Text Acaulide, an Osteogenic Macrodiolide from Acaulium sp. H‑JQSF, an Isopod-Associated Fungus
by Wang, Ting Ting and Wei, Ying Jie and Ge, Hui Ming and Jiao, Rui Hua and Tan, Ren Xiang
Organic Letters, ISSN 1523-7060, 02/2018, Volume 20, Issue 4, pp. 1007 - 1010
Acaulide (1), a macrodiolide with an unprecedented framework, was characterized along with its shunt productsacaulones A (2) and B (3)from the culture of... 
CHEMISTRY, ORGANIC | CLONOSTACHYDIOL | ABSOLUTE-CONFIGURATION | DALDINIA-ESCHSCHOLZII | OSTEOPOROSIS
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16. Full Text Analysis of Configuration and Conformation of Furanose Ring in Carbohydrate and Nucleoside by Vibrational Circular Dichroism
by Taniguchi, Tohru and Nakano, Kie and Baba, Ryosuke and Monde, Kenji
Organic Letters, ISSN 1523-7060, 01/2017, Volume 19, Issue 2, pp. 404 - 407
A reliable and convenient method for determining the configuration and conformation of the furanose ring in carbohydrates and nucleosides by vibrational... 
CHEMISTRY, ORGANIC | NUCLEOTIDES | DUPLEXES | ABSOLUTE-CONFIGURATION | SPECTROSCOPY | VCD
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17. Full Text Organocatalytic asymmetric hydrophosphonylation/Mannich reactions using thiourea, cinchona and brnsted acid catalysts
by Bhadury, Pinaki S and Li, Hu
Synlett, ISSN 0936-5214, 2012, Volume 23, Issue 8, pp. 1108 - 1131
enantioselectivity | chirality | Brnsted acids | diastereoselectivity | organocatalysts | absolute configuration
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18. Full Text Lentiquinones A, B, and C, Phytotoxic Anthraquinone Derivatives Isolated from Ascochyta lentis, a Pathogen of Lentil
by Masi, Marco and Nocera, Paola and Zonno, Maria C and Tuzi, Angela and Pescitelli, Gennaro and Cimmino, Alessio and Boari, Angela and Infantino, Alessandro and Vurro, Maurizio and Evidente, Antonio
Journal of Natural Products, ISSN 0163-3864, 12/2018, Volume 81, Issue 12, pp. 2700 - 2709
A strain of the pathogenic fungus Ascochyta lentis isolated from lentil (Lens culinaris) was studied to ascertain its capability to produce bioactive... 
ASSIGNMENT | PHARMACOLOGY & PHARMACY | CHEMISTRY, MEDICINAL | ABSOLUTE-CONFIGURATION | PLANT SCIENCES
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19. Full Text Sesquiterpenoids from Artemisia vestita and Their Antifeedant and Antifungal Activities
by Ding, Ying-Hui and Wang, Hui-Ting and Shi, Sha and Meng, Yao and Feng, Jin-Chao and Wu, Hai-Bo
Molecules, ISSN 1420-3049, 10/2019, Volume 24, Issue 20, p. 3671
Four new sesquiterpenoids, named artemivestinolide D–G (1–4) and three known sesquiterpenoids (5–7), were isolated from Artemisia vestita. The structures of... 
antifeedant | antifungal | sesquiterpenoids | absolute configuration | Artemisia vestita
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20. Full Text Antiviral Spirotriscoumarins A and B: Two Pairs of Oligomeric Coumarin Enantiomers with a Spirodienone–Sesquiterpene Skeleton from Toddalia asiatica
by Tang, Zhong-Hai and Liu, Yun-Bao and Ma, Shuang-Gang and Li, Li and Li, Yong and Jiang, Jian-Dong and Qu, Jing and Yu, Shi-Shan
Organic Letters, ISSN 1523-7060, 10/2016, Volume 18, Issue 19, pp. 5146 - 5149
Two pairs of oligomeric coumarin enantiomers, spirotriscoumarin A [(+)-1 and (−)-1] and spirotriscoumarin B [(+)-2 and (−)-2], with a... 
CHEMISTRY, ORGANIC | ACID | INHIBITORS | ABSOLUTE-CONFIGURATION | GRISEOFULVIN | DERIVATIVES
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