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Superacidic Cyclization of Bicyclogeranylfarnesic and Geranylfarnesic Acids and their Esters

Pavel Fedorovich Vlad 1
Pavel Fedorovich Vlad
, 
Nicon D Ungur 1
Nicon D Ungur
, 
Nguen Van Tuen 1
Nguen Van Tuen
10.1070/MC1992v002n02ABEH000134
Published 1992-06-30
Communication , Volume 2, Issue 2, 61-62
3
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Vlad P. F., Ungur N. D., Tuen N. V. Superacidic Cyclization of Bicyclogeranylfarnesic and Geranylfarnesic Acids and their Esters // Mendeleev Communications. 1992. Vol. 2. No. 2. pp. 61-62.
GOST all authors (up to 50) Copy
Vlad P. F., Ungur N. D., Tuen N. V. Superacidic Cyclization of Bicyclogeranylfarnesic and Geranylfarnesic Acids and their Esters // Mendeleev Communications. 1992. Vol. 2. No. 2. pp. 61-62.
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TY - JOUR
DO - 10.1070/MC1992v002n02ABEH000134
UR - https://mendcomm.colab.ws/publications/10.1070/MC1992v002n02ABEH000134
TI - Superacidic Cyclization of Bicyclogeranylfarnesic and Geranylfarnesic Acids and their Esters
T2 - Mendeleev Communications
AU - Vlad, Pavel Fedorovich
AU - Ungur, Nicon D
AU - Tuen, Nguen Van
PY - 1992
DA - 1992/06/30
PB - Mendeleev Communications
SP - 61-62
IS - 2
VL - 2
ER -
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@article{1992_Vlad,
author = {Pavel Fedorovich Vlad and Nicon D Ungur and Nguen Van Tuen},
title = {Superacidic Cyclization of Bicyclogeranylfarnesic and Geranylfarnesic Acids and their Esters},
journal = {Mendeleev Communications},
year = {1992},
volume = {2},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1992v002n02ABEH000134},
number = {2},
pages = {61--62},
doi = {10.1070/MC1992v002n02ABEH000134}
}
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Vlad, Pavel Fedorovich, et al. “Superacidic Cyclization of Bicyclogeranylfarnesic and Geranylfarnesic Acids and their Esters.” Mendeleev Communications, vol. 2, no. 2, Jun. 1992, pp. 61-62. https://mendcomm.colab.ws/publications/10.1070/MC1992v002n02ABEH000134.

Abstract

An effective structure-selective stereospecific synthesis of tetracyclic scalarane esters 6 and 7 from bicyclic 2–5 and aliphatic 8–11 precursors has been accomplished.

References

1.
Sesterterpenoids
Hanson J.R.
Natural Product Reports, 1986
2.
Biogenetic-type synthesis of scalaranes
Herz W., Prasad J.S.
Journal of Organic Chemistry, 1982
3.
Biogenetic - Type Synthesis of 12,16 - Deoxyfuroscalarol
Herz W., Prasad J.S.
Synthetic Communications, 1983
6.
Total syntheses of marine sponge metabolites. Part 3. Stereoselective total synthesis of (±)-12-deoxyscalaradial
Nakano T., Hernández M.I., Martín A., Medina J.D.
Journal of the Chemical Society Perkin Transactions 1, 1988
7.
10.1070/MC1992v002n02ABEH000134_bib7
Vlad
Khim. Prir. Soedin., 1988
8.
10.1070/MC1992v002n02ABEH000134_bib8
Vlad
Khim. Prir. Soedin., 1988