2 article(s) from Uchiyama, Masanobu
The regio- and stereoselectivity in quiannulatene and sesterfisherol biosynthesis are determined by...
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Reaction mechanism of quiannulatene biosynthesis. GFPP: geranylfarnesyl diphosphate, IM: intermedia...
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Reaction mechanisms of sesterfisherol biosynthesis. Sesterfisherol is formed by the hydration of IM...
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Energy diagram and heat map analysis of 5/12/5 tricycle formation (A) IM1–IM4 in quiannulatene bios...
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Energy diagram and heat map analysis of conformational change and hydrogen shift (A) IM4–IM6e in qu...
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Energy diagram and heat map analysis of ring rearrangement (A) IM6e–IM11 in quiannulatene biosynthe...
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Beilstein J. Org. Chem. 2019, 15, 1890–1897, doi:10.3762/bjoc.15.184
Phosphole-based tetracyclic heteroacenes.
Synthesis of benzophospholo[3,2-b]indole 3.
Chemical modifications of the phosphorus atom of 3.
ORTEP drawing of compound 3 (left) and 4 (right) with 50% probability. All hydrogen atoms are omitt...
UV–vis absorption (left) and normalized fluorescence emission (right, excitation at 335 nm) spectra...
The spatial plots of the HOMO and LUMO of compounds 3, 4, 7 and 9. The calculations were performed ...
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The spatial plots of the selected molecular orbitals of compounds 5 and 6. The calculations were pe...
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Beilstein J. Org. Chem. 2017, 13, 2304–2309, doi:10.3762/bjoc.13.226
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