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Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone

Alevtina Mikhailovna Turuta 1
Alevtina Mikhailovna Turuta
, 
Alexey Vladimirovich Kamernitskii 1
Alexey Vladimirovich Kamernitskii
, 
Tat'yana Mikhailovna Fadeeva 1
Tat'yana Mikhailovna Fadeeva
, 
Luu Duc Huy 1
Luu Duc Huy
10.1070/MC1992v002n02ABEH000123
Published 1992-06-30
Communication , Volume 2, Issue 2, 47-48
2
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Turuta A. M. et al. Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone // Mendeleev Communications. 1992. Vol. 2. No. 2. pp. 47-48.
GOST all authors (up to 50) Copy
Turuta A. M., Kamernitskii A. V., Fadeeva T. M., Huy L. D. Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone // Mendeleev Communications. 1992. Vol. 2. No. 2. pp. 47-48.
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TY - JOUR
DO - 10.1070/MC1992v002n02ABEH000123
UR - https://mendcomm.colab.ws/publications/10.1070/MC1992v002n02ABEH000123
TI - Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone
T2 - Mendeleev Communications
AU - Turuta, Alevtina Mikhailovna
AU - Kamernitskii, Alexey Vladimirovich
AU - Fadeeva, Tat'yana Mikhailovna
AU - Huy, Luu Duc
PY - 1992
DA - 1992/06/30
PB - Mendeleev Communications
SP - 47-48
IS - 2
VL - 2
ER -
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@article{1992_Turuta,
author = {Alevtina Mikhailovna Turuta and Alexey Vladimirovich Kamernitskii and Tat'yana Mikhailovna Fadeeva and Luu Duc Huy},
title = {Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone},
journal = {Mendeleev Communications},
year = {1992},
volume = {2},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1992v002n02ABEH000123},
number = {2},
pages = {47--48},
doi = {10.1070/MC1992v002n02ABEH000123}
}
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Turuta, Alevtina Mikhailovna, et al. “Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone.” Mendeleev Communications, vol. 2, no. 2, Jun. 1992, pp. 47-48. https://mendcomm.colab.ws/publications/10.1070/MC1992v002n02ABEH000123.

Abstract

An effective synthesis of 16α, 17α-epoxycorticosterone from androsta-4,9-diene-3,17-dione via 17α-ethynylandrost-4-ene-11β,17β-diol-3-one has been developed.

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