1. Journal of Chemical Society, 1945, 277 - 280
Synthetical and stereochemical investigations of reduced cyclic bases. Part I. Hydrogenation products of indole and the exhaustive methylation of an N-methyloctahydroindole
F. E. King, J. A. Barltrop and R. J. Walley
Код: Выделить всё
http://dx.doi.org/10.1039/JR9450000277New syntheses of DL-tryptophan. Part I. Syntheses from ethyl -aceto--3-indolylpropionate and ethyl -cyano--3-indolylpropionate
D. O. Holland and J. H. C. Nayler
Код: Выделить всё
http://dx.doi.org/10.1039/JR9530000280Synthetic and stereochemical investigations of reduced cyclic bases. Part VI. A new synthesis of trans-octahydroindole and a re-investigation of its Hofmann methylation products
H. Booth and F. E. King
Код: Выделить всё
http://dx.doi.org/10.1039/JR9580002688-Amino--keto-acids. Part I. Synthesis and attempted isolation of the free acids
W. G. Laver, A. Neuberger and J. J. Scott
Код: Выделить всё
http://dx.doi.org/10.1039/JR9590001474Sur quelques derives de l'oxindole et de l'isatine. II. Sur les amino-, hydroxy- et methoxy-derives substitues en position 5 et 6
Edgardo Giovannini, Plato Portmann
Код: Выделить всё
http://dx.doi.org/10.1002/hlca.19480310524Reduction of some 2,3-diaryl cyclohexanones and their oximes.
N. Arumugam and P. Shenbagamurthi
Код: Выделить всё
http://dx.doi.org/10.1016/S0040-4039(01)84818-8Reduktion von Ketoximen mit Zinkstaub in ammoniakalischer Losung
Johannes C. Jochims1
Код: Выделить всё
http://dx.doi.org/10.1007/BF00913069