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- W1966831362 abstract "THE structures of the two stereoisomeric hydrogenation products of naphthalene and their relationship to cyclohexane were discussed by one of us in 19431. It was pointed out that the trans structure proposed by Mohr2 (Fig. 1) will probably be correct, but reasons were given indicating that Mohr's cis structure containing two cyclohexane rings of the 'cradle' form should be rejected in favour of another structure shown in Fig. 1,b. The carbon skeleton of both these two molecules is found in the well-known diamond lattice. Using the notation introduced in a paper dealing with the cyclohexane problem3, the two cyclohexane rings of trans-decahn may be said to share two x-bonds; in cis-decalin, however, one x-bond and one?-bond." @default.
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- W1966831362 date "1946-06-08" @default.
- W1966831362 modified "2023-09-23" @default.
- W1966831362 title "Structure of the So-called cis Decalin" @default.
- W1966831362 doi "https://doi.org/10.1038/157765a0" @default.
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