has been cited by the following article(s):
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[1]
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(2R?, 3S?, 4S?, 2 ″R?, 3 ″S?)-Guibourtinidol-(4α→ 8)-catechin, a biflavanoid procyanidin of the proguibourtinidin group from Senna macranthera: its relative stereochemistry and conformation
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Tetrahedron: Asymmetry,
2015 |
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[2]
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Carboxy Methyl and Carboxy Analogs Argaminolics B and C.
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Records of Natural Products,
2015 |
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[3]
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Carboxy Methyl and Carboxy Analogs Argaminolics B and C
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Rec. Nat. Prod,
2015 |
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[4]
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(2R∗, 3S∗, 4S∗, 2 ″R∗, 3 ″S∗)-Guibourtinidol-(4α→ 8)-catechin, a biflavanoid procyanidin of the proguibourtinidin group from Senna macranthera: its relative …
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Tetrahedron: Asymmetry,
2015 |
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[5]
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Epimers vs. inverse epimers: the C-1 configuration in alnumycin A1
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RSC Advances,
2012 |
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[6]
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Alnumycins A2 and A3: new inverse-epimeric pairs stereoisomeric to alnumycin A1
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Tetrahedron: Asymmetry,
2012 |
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[7]
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The potential of VCD to resolve the epimer vs. inverse epimer quandary
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Computational and Theoretical Chemistry? ,
2012 |
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[8]
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Chiral Solid Solutions for the NMR Analysis of Enantiomers: A Potential New Approach to Chiral Analysis
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Journal of Spectroscopy,
2012 |
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[9]
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Suggested new terms for describing chiral states and the state-dependent behavior of chiral systems
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International Journal of Organic Chemistry,
2012 |
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[10]
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Application of the PROJECT Concept for Suppression of J Modulation to DEPT for 13C-Multilabeled Analytes
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Organic letters,
2011 |
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[1]
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(2R∗,3S∗,4S∗,2″R∗,3″S∗)-Guibourtinidol-(4α→8)-catechin, a biflavanoid procyanidin of the proguibourtinidin group from Senna macranthera: its relative stereochemistry and conformation
Tetrahedron: Asymmetry,
2015
DOI:10.1016/j.tetasy.2015.01.013
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[2]
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Chiral Solid Solutions for the NMR Analysis of Enantiomers: A Potential New Approach to Chiral Analysis
Journal of Spectroscopy,
2013
DOI:10.1155/2013/970654
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[3]
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The potential of VCD to resolve the epimer vs. inverse epimer quandary
Computational and Theoretical Chemistry,
2012
DOI:10.1016/j.comptc.2012.05.031
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[4]
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Alnumycins A2 and A3: new inverse-epimeric pairs stereoisomeric to alnumycin A1
Tetrahedron: Asymmetry,
2012
DOI:10.1016/j.tetasy.2012.05.001
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[5]
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Epimers vs. inverse epimers: the C-1 configuration in alnumycin A1
RSC Advances,
2012
DOI:10.1039/c2ra20537h
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[6]
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Suggested New Terms for Describing Chiral States and the State-Dependent Behavior of Chiral Systems
International Journal of Organic Chemistry,
2012
DOI:10.4236/ijoc.2012.23031
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[7]
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Application of the PROJECT Concept for Suppression of J Modulation to DEPT for 13C-Multilabeled Analytes
Organic Letters,
2012
DOI:10.1021/ol2031334
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