Fig. 2. Synthesis and reactions of α-pinene. Biosynthetic pathway (orange); Synthetic starting point for α-pinene synthesis (red); Phytochemicals (green); Insecticides and herbicides (blue); References [a]: (Upshur et al., 2019); [b-c]: (Liu et al., 2008; Prakoso et al., 2018; Wr´oblewska et al., 2018); [d]: (Dong et al., 2020); [e]: (Xu et al., 2020). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)Published as part of Allenspach, Martina & Steuer, Christian, 2021, α-Pinene: A never-ending story, pp. 1-7 in Phytochemistry (112857) 190 on page 4, DOI: 10.1016/j.phytochem.2021.112857, http://zenodo.org/record/825753
Fig. 2. Putative camphor biosynthesis pathway. Schematic representation of the putative camphor bios...
Fig. 3. Hybrid quadrupole-orbitrap GC-MS/MS. a shows the chromatogram of terpene products of F482L. ...
Fig. 22. Postulated biogenetic pathway for ochraceopones A-E (234–238).Published as part of Zhao, We...
Fig. 1. a, The proposed reaction mechanism for the synthesis of limonene, pinene and sabinene. b, Th...
Fig. 1. Chemical structures of the pinenes with their two enantiomers: (+)-α-pinene (1), ()-α-pinene...
Allenspach, Martina, Steuer, Christian (2021): α-Pinene: A never-ending story. Phytochemistry (11285...
Fig. 3. Theorised monoterpenoid biosynthesis pathway. Compounds highlighted in blue comprise the γ-t...
Fig. 2. Converting pinene synthase to sabinene synthase by mutations on 482 position. Chromatograms ...
Fig. 23. Reaction catalyzed by NDC1/demethylphylloquinone reductase. The penultimate step in the bio...
Fig. 2. Proposed metabolic network of isoquinoline alkaloids in the Macleaya genus. a the solid arro...
Fig. 2. Molecular structure of Gt5,3′ acyltransferase. The structure is depicted by a ribbon model. ...
Fig. 1. Biosynthesis pathway proposal for disubstituted tricycloalternarenes.Published as part of Fr...
Fig. 1. The proposed carboxyl group formation of celastrol at the C-29 position and carboxyl group f...
Fig. 4. Conformational differences in the pinyl cation in WT and F482Y as demonstrated by molecular ...
Fig. 5. The effect of the S491A mutation. Chromatograms in a, b and c show the GC-MS analysis of ter...
Fig. 2. Putative camphor biosynthesis pathway. Schematic representation of the putative camphor bios...
Fig. 3. Hybrid quadrupole-orbitrap GC-MS/MS. a shows the chromatogram of terpene products of F482L. ...
Fig. 22. Postulated biogenetic pathway for ochraceopones A-E (234–238).Published as part of Zhao, We...
Fig. 1. a, The proposed reaction mechanism for the synthesis of limonene, pinene and sabinene. b, Th...
Fig. 1. Chemical structures of the pinenes with their two enantiomers: (+)-α-pinene (1), ()-α-pinene...
Allenspach, Martina, Steuer, Christian (2021): α-Pinene: A never-ending story. Phytochemistry (11285...
Fig. 3. Theorised monoterpenoid biosynthesis pathway. Compounds highlighted in blue comprise the γ-t...
Fig. 2. Converting pinene synthase to sabinene synthase by mutations on 482 position. Chromatograms ...
Fig. 23. Reaction catalyzed by NDC1/demethylphylloquinone reductase. The penultimate step in the bio...
Fig. 2. Proposed metabolic network of isoquinoline alkaloids in the Macleaya genus. a the solid arro...
Fig. 2. Molecular structure of Gt5,3′ acyltransferase. The structure is depicted by a ribbon model. ...
Fig. 1. Biosynthesis pathway proposal for disubstituted tricycloalternarenes.Published as part of Fr...
Fig. 1. The proposed carboxyl group formation of celastrol at the C-29 position and carboxyl group f...
Fig. 4. Conformational differences in the pinyl cation in WT and F482Y as demonstrated by molecular ...
Fig. 5. The effect of the S491A mutation. Chromatograms in a, b and c show the GC-MS analysis of ter...
Fig. 2. Putative camphor biosynthesis pathway. Schematic representation of the putative camphor bios...
Fig. 3. Hybrid quadrupole-orbitrap GC-MS/MS. a shows the chromatogram of terpene products of F482L. ...
Fig. 22. Postulated biogenetic pathway for ochraceopones A-E (234–238).Published as part of Zhao, We...