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Q48236797-3CE44B3D-AB92-4A35-9F6C-28B57D3EB41B
Q48236797-3CE44B3D-AB92-4A35-9F6C-28B57D3EB41B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48236797-3CE44B3D-AB92-4A35-9F6C-28B57D3EB41B
Structural revision of two unusual rhamnofolane diterpenes, curcusones I and J, by means of DFT calculations of NMR shifts and coupling constants.
P2860
Q48236797-3CE44B3D-AB92-4A35-9F6C-28B57D3EB41B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48236797-3CE44B3D-AB92-4A35-9F6C-28B57D3EB41B
rank
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type
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wasDerivedFrom
2d014ffe04c847dbe6a11aea2c46eec4a6fcf6ac
P2860
Synergy of synthesis, computation and NMR reveals correct baulamycin structures.