HUANG-MINLON JOHN BABCOCK, . ISOMERIZATION AND DISPLACEMENT REACTIONS IN THE CYANOPREGNENE SERIES.SYNTHESIS OF 17-HYDRO-XYDEHYDRO CORTICOSTERONE 21-METHYL ETHERJ. Acta Pharmaceutica Sinica, 1955, 3(1): 39-49.
Citation:
HUANG-MINLON JOHN BABCOCK, . ISOMERIZATION AND DISPLACEMENT REACTIONS IN THE CYANOPREGNENE SERIES.SYNTHESIS OF 17-HYDRO-XYDEHYDRO CORTICOSTERONE 21-METHYL ETHERJ. Acta Pharmaceutica Sinica, 1955, 3(1): 39-49.
HUANG-MINLON JOHN BABCOCK, . ISOMERIZATION AND DISPLACEMENT REACTIONS IN THE CYANOPREGNENE SERIES.SYNTHESIS OF 17-HYDRO-XYDEHYDRO CORTICOSTERONE 21-METHYL ETHERJ. Acta Pharmaceutica Sinica, 1955, 3(1): 39-49.
Citation:
HUANG-MINLON JOHN BABCOCK, . ISOMERIZATION AND DISPLACEMENT REACTIONS IN THE CYANOPREGNENE SERIES.SYNTHESIS OF 17-HYDRO-XYDEHYDRO CORTICOSTERONE 21-METHYL ETHERJ. Acta Pharmaceutica Sinica, 1955, 3(1): 39-49.
ISOMERIZATION AND DISPLACEMENT REACTIONS IN THE CYANOPREGNENE SERIES.SYNTHESIS OF 17-HYDRO-XYDEHYDRO CORTICOSTERONE 21-METHYL ETHER
20-cyano-17-pregnene-3(u),21-diol-11-one has baen found to undergo geome- trical inversion under alkaline conditions accompanied by ether formation at position 21.This discovery has enabled the synthesis of 17-hydroxydehydrocorticosterone 21-methyl ether.