The preparation of 14-hydroxylated yohimbine and reserpine derivatives.
Publication type: Journal Article
Publication date: 2011-12-08
scimago Q3
wos Q3
SJR: 0.349
CiteScore: 2.7
Impact factor: 1.3
ISSN: 00092363, 13475223
General Chemistry
Drug Discovery
General Medicine
Abstract
Hydroxylation at C-14 of yohimbine (6), pseudoyohimbine (7) and isoreserpine (8) was made through oxidation of the enamines (10, 15) with benzoyl or p-nitrobenzoyl peroxide followed by reduction with NaBH4 and removal of benzoyl or p-nitrobenzoyl group to give the 14-hydroxylated compounds (13, 14, 22).
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Total citations:
14
Citations from 2024:
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GOST
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YAMANAKA E. et al. The preparation of 14-hydroxylated yohimbine and reserpine derivatives. // Chemical and Pharmaceutical Bulletin. 2011. Vol. 32. No. 2. pp. 818-821.
GOST all authors (up to 50)
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YAMANAKA E., Ono M., Kasamatsu S., Aimi N., Sakai S. The preparation of 14-hydroxylated yohimbine and reserpine derivatives. // Chemical and Pharmaceutical Bulletin. 2011. Vol. 32. No. 2. pp. 818-821.
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RIS
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TY - JOUR
DO - 10.1248/cpb.32.818
UR - https://doi.org/10.1248/cpb.32.818
TI - The preparation of 14-hydroxylated yohimbine and reserpine derivatives.
T2 - Chemical and Pharmaceutical Bulletin
AU - YAMANAKA, ETSUJI
AU - Ono, Machiko
AU - Kasamatsu, Satoe
AU - Aimi, Norio
AU - Sakai, Shinichiro
PY - 2011
DA - 2011/12/08
PB - Pharmaceutical Society of Japan
SP - 818-821
IS - 2
VL - 32
SN - 0009-2363
SN - 1347-5223
ER -
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BibTex (up to 50 authors)
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@article{2011_YAMANAKA,
author = {ETSUJI YAMANAKA and Machiko Ono and Satoe Kasamatsu and Norio Aimi and Shinichiro Sakai},
title = {The preparation of 14-hydroxylated yohimbine and reserpine derivatives.},
journal = {Chemical and Pharmaceutical Bulletin},
year = {2011},
volume = {32},
publisher = {Pharmaceutical Society of Japan},
month = {dec},
url = {https://doi.org/10.1248/cpb.32.818},
number = {2},
pages = {818--821},
doi = {10.1248/cpb.32.818}
}
Cite this
MLA
Copy
YAMANAKA, ETSUJI, et al. “The preparation of 14-hydroxylated yohimbine and reserpine derivatives..” Chemical and Pharmaceutical Bulletin, vol. 32, no. 2, Dec. 2011, pp. 818-821. https://doi.org/10.1248/cpb.32.818.