Absolute configuration of cis- and trans-2-(o-bromophenyl)cyclohexylamine and related compounds

1976 ◽  
Vol 41 (9) ◽  
pp. 1640-1642 ◽  
Author(s):  
Todd G. Cochran ◽  
Allan. Weber ◽  
Alain C. Huitric ◽  
Arthur. Camerman ◽  
Lyle H. Jensen
Keyword(s):  
Absolute Configuration ◽  
Cis And Trans ◽  
Related Compounds

scholarly journals Botrylactone: new interest in an old molecule—review of its absolute configuration and related compounds

Tetrahedron ◽  
2011 ◽  
Vol 67 (2) ◽  
pp. 417-420 ◽  
Author(s):  
Javier Moraga ◽  
Cristina Pinedo ◽  
Rosa Durán-Patrón ◽  
Isidro G. Collado ◽  
Rosario Hernández-Galán
Keyword(s):  
Absolute Configuration ◽  
Related Compounds

Juglomycins G-J: Isolation from Streptomycetes and Structure Elucidation

2005 ◽  
Vol 60 (2) ◽  
pp. 183-188 ◽  
Author(s):  
R. P. Maskey ◽  
H. Lessmann ◽  
S. Fotso ◽  
I. Grün-Wollny ◽  
H. Lackner ◽  
...  
Keyword(s):  
Antibacterial Activity ◽  
Absolute Configuration ◽  
Structure Elucidation ◽  
Mass Spectra ◽  
2D Nmr ◽  
Cd Spectra ◽  
Streptomyces Spp ◽  
Nmr Data ◽  
Related Compounds ◽  
Weak Antibacterial Activity

From the Streptomyces spp. 815 and GW4184, four new 4-juglon-2-ylbutyric acid derivatives, the juglomycins G - J (3a, 4a, 4c, 5c), have been isolated and characterised. The structures were derived from the 1D and 2D NMR data and mass spectra and confirmed by comparison with structurally related compounds. The absolute configuration was deduced from the CD spectra. The new natural products exhibited weak antibacterial activity similar to juglomycin A (5a).

Synthesis of cis- and trans-2-Phenoxycyclopropylamines and Related Compounds

1965 ◽  
Vol 8 (4) ◽  
pp. 432-439 ◽  
Author(s):  
Jacob Finkelstein ◽  
Elliot Chiang ◽  
John Lee
Keyword(s):  
Cis And Trans ◽  
Related Compounds

Molecular Structure of cis- and trans-Tergurides

1998 ◽  
Vol 63 (3) ◽  
pp. 425-433 ◽  
Author(s):  
Michal Hušák ◽  
Bohumil Kratochvíl ◽  
Petr Sedmera ◽  
Vladimír Havlíček ◽  
Hana Votavová ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Crystal Structure ◽  
Absolute Configuration ◽  
Catalytic Hydrogenation ◽  
Ergot Alkaloid ◽  
Cd Spectra ◽  
X Ray ◽  
Relative Stereochemistry ◽  
Cis And Trans

Four isomers of terguride, a semisynthetic ergot alkaloid derivative, have been prepared by catalytic hydrogenation of (5R,8S)- and (5S,8S)-lisuride [1,1-diethyl-3-(6-methyl-8-ergolenyl)urea]. Relative stereochemistry of the isomers is based on NMR and CD spectra. Absolute configuration of all the series has been confirmed by the X-ray crystal structure determination of (5R,8S,10S)-terguride 2-bromobenzoate [1,1-diethyl-3-(6-methyl-8-isoergolenyl)urea, cis-dihydrolisuride].

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