One-Pot Synthesis ofN-Protected β-Chiral Amino Alcohols
Publication type: Journal Article
Publication date: 2003-06-10
scimago Q3
wos Q3
SJR: 0.322
CiteScore: 4.3
Impact factor: 1.8
ISSN: 00397911, 15322432
Organic Chemistry
Abstract
N-tert-butyloxycarbonyl-S-benzyl-cysteine, N-fluorenylmethyloxy-carbonyl-alanine-, S-trityl-cysteine-, O-tert-butyl-serine- and O-tert-butyl-tyrosine were converted to the corresponding alcohols via sodium borohydride reduction of their in situ formed methyl esters. Enantiopurity of the products was checked by chiral HPLC method.
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12
Total citations:
12
Citations from 2025:
1
(8.33%)
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GOST
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Somlai C. et al. One-Pot Synthesis ofN-Protected β-Chiral Amino Alcohols // Synthetic Communications. 2003. Vol. 33. No. 11. pp. 1815-1820.
GOST all authors (up to 50)
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Somlai C., Antal P., Forgó P., Penke B. One-Pot Synthesis ofN-Protected β-Chiral Amino Alcohols // Synthetic Communications. 2003. Vol. 33. No. 11. pp. 1815-1820.
Cite this
RIS
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TY - JOUR
DO - 10.1081/scc-120020188
UR - https://doi.org/10.1081/scc-120020188
TI - One-Pot Synthesis ofN-Protected β-Chiral Amino Alcohols
T2 - Synthetic Communications
AU - Somlai, Csaba
AU - Antal, Péter
AU - Forgó, Peter
AU - Penke, Botond
PY - 2003
DA - 2003/06/10
PB - Taylor & Francis
SP - 1815-1820
IS - 11
VL - 33
SN - 0039-7911
SN - 1532-2432
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2003_Somlai,
author = {Csaba Somlai and Péter Antal and Peter Forgó and Botond Penke},
title = {One-Pot Synthesis ofN-Protected β-Chiral Amino Alcohols},
journal = {Synthetic Communications},
year = {2003},
volume = {33},
publisher = {Taylor & Francis},
month = {jun},
url = {https://doi.org/10.1081/scc-120020188},
number = {11},
pages = {1815--1820},
doi = {10.1081/scc-120020188}
}
Cite this
MLA
Copy
Somlai, Csaba, et al. “One-Pot Synthesis ofN-Protected β-Chiral Amino Alcohols.” Synthetic Communications, vol. 33, no. 11, Jun. 2003, pp. 1815-1820. https://doi.org/10.1081/scc-120020188.