ChemInform Abstract: Fungal Metabolites. Part 22. Determination of Absolute Configuration and Biological Activity of New Immunosuppressants, Mycestericins D, E, F, and G.

T. FUJITA; N. HAMAMICHI; M. KIUCHI; T. MATSUZAKI; Y. KITAO; K. INOUE; R. HIROSE; M. YONETA; S. SASAKI; K. CHIBA

doi:10.1002/chin.199712226

ChemInform Abstract: Fungal Metabolites. Part 22. Determination of Absolute Configuration and Biological Activity of New Immunosuppressants, Mycestericins D, E, F, and G.

ChemInform ◽

10.1002/chin.199712226 ◽

2010 ◽

Vol 28 (12) ◽

pp. no-no

Author(s):

T. FUJITA ◽

N. HAMAMICHI ◽

M. KIUCHI ◽

T. MATSUZAKI ◽

Y. KITAO ◽

...

Keyword(s):

Biological Activity ◽

Absolute Configuration ◽

Fungal Metabolites ◽

Determination Of Absolute Configuration

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Determination of Absolute Configuration and Biological Activity of New Immunosuppressants, Mycestericins D, E, F and G.

The Journal of Antibiotics ◽

10.7164/antibiotics.49.846 ◽

1996 ◽

Vol 49 (9) ◽

pp. 846-853 ◽

Cited By ~ 43

Author(s):

TETSURO FUJITA ◽

NORIMITSU HAMAMICHI ◽

MASATOSHI KIUCHI ◽

TOHRU MATSUZAKI ◽

YUKI KITAO ◽

...

Keyword(s):

Biological Activity ◽

Absolute Configuration ◽

Determination Of Absolute Configuration

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Discovery of a pair of diastereomers as potent HDACs inhibitors: determination of absolute configuration, biological activity comparison and computational study

RSC Advances ◽

10.1039/c3ra43249a ◽

2013 ◽

Vol 3 (43) ◽

pp. 21106 ◽

Cited By ~ 2

Author(s):

Yingjie Zhang ◽

Elizabeth S. Inks ◽

Mengyuan Zhu ◽

C. James Chou ◽

Hao Fang ◽

...

Keyword(s):

Biological Activity ◽

Absolute Configuration ◽

Computational Study ◽

Determination Of Absolute Configuration ◽

Activity Comparison

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Sulfoxide Analogs of TAK-875 as G Protein Coupled Receptor 40 Agonists: Synthesis, Determination of Absolute Configuration and Biological Activity

Chinese Journal of Organic Chemistry ◽

10.6023/cjoc201612041 ◽

2017 ◽

Vol 37 (4) ◽

pp. 858 ◽

Cited By ~ 1

Author(s):

Yugang Yan ◽

Xueying Chen ◽

Xinying Yang ◽

Wenfang Xu ◽

Yingjie Zhang

Keyword(s):

Biological Activity ◽

G Protein ◽

Absolute Configuration ◽

G Protein Coupled Receptor ◽

Determination Of Absolute Configuration ◽

G Protein Coupled

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Determination of absolute configuration of chiral molecules using vibrational optical activity

Planta Medica ◽

10.1055/s-0032-1320280 ◽

2012 ◽

Vol 78 (11) ◽

Author(s):

Y He ◽

B Wang ◽

RK Dukor ◽

LA Nafie

Keyword(s):

Optical Activity ◽

Absolute Configuration ◽

Chiral Molecules ◽

Determination Of Absolute Configuration

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On terpenes. CCVII. Contribution to the stereochemistry of substances with daucane skeleton and the determination of absolute configuration of laserpitin

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19703597 ◽

1970 ◽

Vol 35 (12) ◽

pp. 3597-3609 ◽

Cited By ~ 10

Author(s):

M. Holub ◽

J. Tax ◽

P. Sedmera ◽

F. Šorm

Keyword(s):

Absolute Configuration ◽

Determination Of Absolute Configuration

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ChemInform Abstract: Concise Total Synthesis of Albaflavenone Utilizing Sequential Intramolecular Aldol Condensation: Determination of Absolute Configuration.

ChemInform ◽

10.1002/chin.201521228 ◽

2015 ◽

Vol 46 (21) ◽

pp. no-no

Author(s):

Toyoharu Kobayashi ◽

Yutaro Kon ◽

Hideki Abe ◽

Hisanaka Ito

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Aldol Condensation ◽

Determination Of Absolute Configuration

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Prismatomerin, a New Iridoid fromPrismatomeristetrandra. Structure Elucidation, Determination of Absolute Configuration, and Cytotoxicity

Journal of Natural Products ◽

10.1021/np070202+ ◽

2007 ◽

Vol 70 (8) ◽

pp. 1339-1343 ◽

Cited By ~ 29

Author(s):

Karsten Krohn ◽

Dietmar Gehle ◽

Sujit Kumar Dey ◽

Nilufar Nahar ◽

Mohammed Mosihuzzaman ◽

...

Keyword(s):

Absolute Configuration ◽

Structure Elucidation ◽

Determination Of Absolute Configuration

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ChemInform Abstract: Lipase Catalyzed Resolution of α-Hydroxymethyl Sulfones. Determination of Absolute Configuration by Semiempirical Calculation of CD Spectra and Verification by X-Ray Structure Analysis.

ChemInform ◽

10.1002/chin.199806056 ◽

2010 ◽

Vol 29 (6) ◽

pp. no-no

Author(s):

H.-J. GAIS ◽

I. VON DER WEIDEN ◽

J. FLEISCHBAUER ◽

J. ESSER ◽

G. RAABE

Keyword(s):

Structure Analysis ◽

Absolute Configuration ◽

Semiempirical Calculation ◽

Cd Spectra ◽

X Ray ◽

Determination Of Absolute Configuration

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Determination of absolute configuration using vibrational circular dichroism spectroscopy: phenyl glycidic acid derivatives obtained via asymmetric epoxidation using oxone and a keto bile acid

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2005.06.035 ◽

2005 ◽

Vol 16 (15) ◽

pp. 2653-2663 ◽

Cited By ~ 25

Author(s):

Frank J. Devlin ◽

Philip J. Stephens ◽

Olga Bortolini

Keyword(s):

Circular Dichroism ◽

Bile Acid ◽

Absolute Configuration ◽

Circular Dichroism Spectroscopy ◽

Vibrational Circular Dichroism ◽

Asymmetric Epoxidation ◽

Determination Of Absolute Configuration ◽

Circular Dichroïsm

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(-)-Strempeliopine, stereoselective total synthesis and the determination of absolute configuration

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19861731 ◽

1986 ◽

Vol 51 (8) ◽

pp. 1731-1742 ◽

Cited By ~ 6

Author(s):

Josef Hájíček ◽

Jan Trojánek

Keyword(s):

Circular Dichroism ◽

Total Synthesis ◽

Absolute Configuration ◽

Determination Of Absolute Configuration ◽

Natural Base ◽

The Absolute ◽

Circular Dichroïsm

A synthesis of (±)-strempeliopine (II) is described, the key step of which is the stereoselective reductive rearrangement of 18-methylene-1,2-dehydroaspidospermidine (XI). The absolute configuration of the natural (-)-base II was determined as (2S, 7R, 20R, 21R) on the basis of its synthesis from (+)-18-methylenevincadifformine (XVII) the configuration of which was derived from a comparison of circular dichroism properties of bases with a β-anilinoacrylate chromophore. The biogenesis of the alkaloids of the schizozygane type is discussed.

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