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4
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0000734627
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Tallent W.H., Stromberg V.L., Horning E.C., J. Am. Chem. Soc. 1955, 77, 6361-6364; Tallent W.H., Horning E.C., ibid. 1956, 78, 4467-4469; Hill R.K., Chan T.H., Joule J.A., Tetrahedron 1965, 21, 147-161.
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5
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0000760852
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Tallent W.H., Stromberg V.L., Horning E.C., J. Am. Chem. Soc. 1955, 77, 6361-6364; Tallent W.H., Horning E.C., ibid. 1956, 78, 4467-4469; Hill R.K., Chan T.H., Joule J.A., Tetrahedron 1965, 21, 147-161.
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Tallent, W.H.1
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6
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0013775371
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Hill, R.K.1
Chan, T.H.2
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7
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0000346930
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The first asymmetric synthesis of (-)-pinidine and (+)-pinidine
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9
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0019803843
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Spande T.F., Daly J.W., Hart D.J., Tsai Y.-M., Macdonald T.L., Experientia 1981, 37, 1242-1245.
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10
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0025041475
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12
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33748647052
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Momose T., Toshima M., Toyooka N., Hirai Y., Eugster C. H., J. Chem. Soc., Perkin Trans. 1 1997, 1307-1314.
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13
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33748651908
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14
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0001762573
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15
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0028291746
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Koga, K.7
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16
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0013564617
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-
+): 351.1504, found 351.1496.
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+): 351.1504, found 351.1496.
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17
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0013564419
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The conditions for HPLC analysis: DAICEL CHIRALPAC AS, hexane / i-PrOH = 10 / 1.
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The conditions for HPLC analysis: DAICEL CHIRALPAC AS, hexane / i-PrOH = 10 / 1.
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-
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18
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0013619526
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11 our group synthesized 18 from 5a in 14 steps with an 8.7% yield. (Formula presented)
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11 our group synthesized 18 from 5a in 14 steps with an 8.7% yield. (Formula presented)
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19
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33947528204
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Ranganathan S., Ranganathan D., Ramachandran P.V., Tetrahedron 1984, 40, 3145-3151.
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Ranganathan, S.1
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Ramachandran, P.V.3
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