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Published in 2021 at "Journal of natural products"
DOI: 10.1021/acs.jnatprod.1c00288
Abstract: Asperspiropene A was originally reported to have a unique 1,8-dioxaspiro[4.5]decane skeleton. During the course of our ongoing research for novel marine natural products, we isolated compound 1, which has identical 1D and 2D NMR data…
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Keywords:
structure revision;
revision asperspiropene;
reisolation structure;
structure ... See more keywords
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Published in 2022 at "Journal of natural products"
DOI: 10.1021/acs.jnatprod.2c00694
Abstract: Balsamisides A-D (1-4) are anti-inflammatory and neurotrophic biflavonoidal glycosides originally proposed to possess an epoxide functionality at the C-2/C-3 position. However, there are inconsistencies in their 13C NMR chemical shift values with those of previously…
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Keywords:
classes biflavonoids;
structure revision;
empirical rule;
13c nmr ... See more keywords
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Published in 2022 at "Journal of natural products"
DOI: 10.1021/acs.jnatprod.2c00828
Abstract: Nordine was reported to be an unusual humulene-type macrocyclic sesquiterpenoid that contains an ether-bridged bicyclic ring between C-10 and C-6 with a hydroxy group at position 2. Here, we report the structure revision of nordine…
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Keywords:
structure;
nordine;
structure revision;
spectroscopic analysis ... See more keywords
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Published in 2019 at "Journal of natural products"
DOI: 10.1021/acs.jnatprod.9b00072
Abstract: The total synthesis of nocarbenzoxazoles F (1) and G (2), originally obtained from the marine-derived halophilic bacterial strain Nocardiopsis lucentensis DSM 44048, was achieved via a simple and versatile route involving microwave-assisted construction of a…
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Keywords:
structure revision;
revision cytotoxicity;
synthesis structure;
structure ... See more keywords
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Published in 2019 at "Chemical Science"
DOI: 10.1039/c8sc05126g
Abstract: Three novel dimeric xanthones, cryptosporioptides A–C were isolated from Cryptosporiopsis sp. 8999 and their structures elucidated.
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Keywords:
revision cryptosporioptides;
genetic basis;
structure revision;
cryptosporioptides determination ... See more keywords
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Published in 2022 at "Natural Product Research"
DOI: 10.1080/14786419.2021.2023867
Abstract: Abstract The structure of an anti-plant pathogenic and plant growth-promoting nonenolide, namely cremenolide, was revised by an efficient combination of DFT-based theoretical NMR calculations and synthesis of a target diastereomer. Initially, the planar structure of…
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Keywords:
structure;
dft nmr;
nmr guided;
structure revision ... See more keywords