Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer
Publication type: Journal Article
Publication date: 1970-07-01
scimago Q2
wos Q3
SJR: 0.620
CiteScore: 4.3
Impact factor: 2.3
ISSN: 0039128X, 18785867
PubMed ID:
5505288
Organic Chemistry
Biochemistry
Molecular Biology
Pharmacology
Clinical Biochemistry
Endocrinology
Abstract
A synthesis of campesteryl acetate and its 24 S epimer has been accomplished starting from the optically active 3,4-dimethylpentylmagnesium bromides and pregnenolone acetate. The two epimers have different utilization by the larvae of Dermestes maculatus .
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IKAN R., Markus A., Bergmann E. D. Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer // Steroids. 1970. Vol. 16. No. 5. pp. 517-522.
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IKAN R., Markus A., Bergmann E. D. Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer // Steroids. 1970. Vol. 16. No. 5. pp. 517-522.
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TY - JOUR
DO - 10.1016/s0039-128x(70)80133-7
UR - https://doi.org/10.1016/s0039-128x(70)80133-7
TI - Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer
T2 - Steroids
AU - IKAN, R.
AU - Markus, A.
AU - Bergmann, E. D.
PY - 1970
DA - 1970/07/01
PB - Elsevier
SP - 517-522
IS - 5
VL - 16
PMID - 5505288
SN - 0039-128X
SN - 1878-5867
ER -
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BibTex (up to 50 authors)
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@article{1970_IKAN,
author = {R. IKAN and A. Markus and E. D. Bergmann},
title = {Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer},
journal = {Steroids},
year = {1970},
volume = {16},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/s0039-128x(70)80133-7},
number = {5},
pages = {517--522},
doi = {10.1016/s0039-128x(70)80133-7}
}
Cite this
MLA
Copy
IKAN, R., et al. “Synthesis of campesteryl acetate ((24R)-24-methyl-3β-acetoxycholesten-5-ene) and its 24S-epimer.” Steroids, vol. 16, no. 5, Jul. 1970, pp. 517-522. https://doi.org/10.1016/s0039-128x(70)80133-7.