2021
DOI: 10.3390/molecules26051423
|View full text |Cite
|
Sign up to set email alerts
|

Enantioselective Synthesis of a New Non-Natural Gabosine

Abstract: The preparation of a new non-natural gabosine is reported, in which the chirality is transferred from the toluene’s biotransformed metabolite (1R,2S)-3-methylcyclohexa-3.5-diene-1,2-diol. Further chemical transformations to introduce additional functionality and chirality to the molecule were also accomplished.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 56 publications
0
1
0
Order By: Relevance
“…S. cellulosae (species and subspecies) have been reported to produce more than 7 useful compounds. Compounds include gabisones, carba sugars, antitumor compound (hexacyclinic acid), proteases, lipases (detergent compatible), phenolic antioxidant compounds, biocontrol compounds ( Ganoderma and Sclerotium rolfsii ), and compounds that induce plant resistance against tobacco mosaic virus ( Ogawara, 1993 ; Regina et al, 2000 ; Muro et al, 2014 ; Rani et al, 2018 ; Attia Abo-Zaid et al, 2020 ; Colobbio et al, 2021 ; Zulfa et al, 2021 ).…”
Section: Discussionmentioning
confidence: 99%
“…S. cellulosae (species and subspecies) have been reported to produce more than 7 useful compounds. Compounds include gabisones, carba sugars, antitumor compound (hexacyclinic acid), proteases, lipases (detergent compatible), phenolic antioxidant compounds, biocontrol compounds ( Ganoderma and Sclerotium rolfsii ), and compounds that induce plant resistance against tobacco mosaic virus ( Ogawara, 1993 ; Regina et al, 2000 ; Muro et al, 2014 ; Rani et al, 2018 ; Attia Abo-Zaid et al, 2020 ; Colobbio et al, 2021 ; Zulfa et al, 2021 ).…”
Section: Discussionmentioning
confidence: 99%