Archiv der Pharmazie p. 35 - 39 (1990)
Update date:2022-08-04
Topics:
Reimann
Speckbacher
Schuenemann
The compounds 4, 8, and 10, prepared by standard methods, are converted to the phenylpyridylakanes 9; their methoiodides 11 are reduced to yield the tetrahydropyridines 12. Whereas the cyclisation of 12a gives the isomers 1f and 1g, 12b furnishes only the
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Doi:10.1021/om100928s
(2011)Doi:10.1021/ja00397a053
(1981)Doi:10.1002/adsc.201000908
(2011)Doi:10.1016/j.poly.2012.06.008
(2013)Doi:10.1111/cbdd.12474
(2015)Doi:10.1016/j.tetlet.2013.02.068
(2013)