A Conformational Study of [3.3](2,6)Pyri
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Sako, Katsuya ;Tatemitsu, Hitoshi ;Onaka, Satoru ;Takemura, Hiroyuki ;Osada, Sat
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Article
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1996
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John Wiley and Sons
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English
⚖ 518 KB
## Abstract A variable‐temperature ^1^H‐NMR study and X‐ray structural analysis show that the most stable conformational isomer of [3.3](2,6)pyridinophane 2 is the __syn__(boat‐boat) conformer, and the relative stability order of the three stable conformers is __syn__(boat‐boat) > __syn__(chair‐boa