Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine
Reference40 articles.
1. A. S. Meyer, M. Hayano, M. C. Lindberg, M. Gut, andO. G. Rodgers, Acta Endocrin.18, 148 (1955).
2. A. S. Meyer, H. Rosenkrantz, andG. Pincus, Amer. Chem. Soc. 126th Meeting, Abstract p. 53–0, New York, 1954.
3. The absence of an isolated olefinic bond in compound VI has been kindly confirmed by Dr.R. Norman Jones who examined the infrared absorption of the compound in chloroform solution with a Perkin-Elmer double-beam spectrophotometer with a sodium chloride prism (R. N. Jones, P. Humphries, E. Packard, andK. Dobriner, J. Amer. Chem. Soc.72, 86 [1950]), and was unable to detect any evidence of an unsaturation other than theΔ 4-bond.
4. TheR-values indicate the mobilities of the substances in the ligroin- and toluene-propylene glycol paper chromatographic system respectively as defined previously (A. S. Meyer, M. Hayano, M. C. Lindberg, M. Gut, andO. G. Rodgers, Acta Endocrin. [l. c.]). For compound II for instance aR lig 2·2 cm/h and for compound IV aR tol 4·0 cm/b have been determined.
5. S. H. Eppstein, P. D. Meister, H. M. Leigh, D. H. Peterson, M. C. Murray, L. M. Reineke, andA. Weintraub, J. Amer. Chem. Soc.76, 3174 (1954).
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