1991
DOI: 10.1055/s-2006-960186
|View full text |Cite
|
Sign up to set email alerts
|

Phytochemical and Biological Study ofSlemmadenia minima

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
6
0

Year Published

1991
1991
2011
2011

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(6 citation statements)
references
References 2 publications
0
6
0
Order By: Relevance
“…Optical rotations, uv, and cd measurements were made in MeOH. Nmr spectra, if not otherwise stated, were recorded in CD3OD with TMS as the internal standard for 'H nmr at 400 MHz and for 1 'C nmr at 100 MHz on a Jeol GX 400 instrument. Ms were run by ei at 70 eV on a Finnigan 4500 instrument and high resolution measurements on a MAT 311.…”
Section: Experimental General Experimentalmentioning
confidence: 99%
See 2 more Smart Citations
“…Optical rotations, uv, and cd measurements were made in MeOH. Nmr spectra, if not otherwise stated, were recorded in CD3OD with TMS as the internal standard for 'H nmr at 400 MHz and for 1 'C nmr at 100 MHz on a Jeol GX 400 instrument. Ms were run by ei at 70 eV on a Finnigan 4500 instrument and high resolution measurements on a MAT 311.…”
Section: Experimental General Experimentalmentioning
confidence: 99%
“…
A novel betaine-type indole alkaloid, 16-e/>z-panarine [1], was isolated from Stemmadenia minima. Its structure was determined by spectral studies and chemical interconver-We recently reported the alkaloid screening of different parts of the Central American plant Stemmadenia minima A. Gentry (Apocynaceae) (1).
…”
mentioning
confidence: 99%
See 1 more Smart Citation
“…Dimethylobovatine [4],-Amorphous compound, [ MHz) 0.89 (6H, dt,7=7.1 Hz, H3-18 and H3-18'), 1.14 (2H, m, Hs-15 and Hs-15'), 1.25 (2H, m, H-20 and H-20'), 1.60 (4H, m, H2-19 and H2-19'), 1.79(2H,m, HK-15 andHR-15'), 1.84(2H, m, Hr-17 and HR-17'), 2.45 (2H, m, Hs-17 and Hs-17'), 2.90 (4H, m, H2-3 and H2-3'), 3.07 (2H, m, Hr-6 and HR-6'), 3.23 (2H, m, HR-5 and HR-5'), 3.27 (2H, m, Hs-6 and Hs-6'), 3.40 (2H, m, Hs-5 and Hs-5'), 3.52 (2H, m, H-21 and H-21'), 3.65 (6H, s, 2 XCOOMe), 3.81 (6H,s, 2 X ArOMe), 6.91 and 6.96 (1H each, d,7=8.3 Hz, H-10 and H-10'), 7.40 (2H, br s, 2XNH), 7.42 and 7.51 (1H each, dj=8.3 Hz, H-9 and H-9')•…”
Section: Methodsmentioning
confidence: 99%
“…Proton-carbon chemical shift correlations for all the carbons directly bonded to protons could be established in an HMQC experiment (Table 2). 134.2 (C-13V149.4 (C-ll) 6.98 (H-10) 124.4 (C-8)/103.1 (C-12) 7.52 (H-9') 134.4 (C-l3')/l53.2 (C-ll') 6.91 (H-10') When compound 2 was methylated with CH2N2 in Et20, the monomethyl derivative 1 and the dimethyl derivative 4 were obtained, confirming chemically the structure of 1. Compound 4 has not been previously found in nature.…”
mentioning
confidence: 99%