Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis: Intramolecular π-Stacking Interactions as a Source of Stereocontrol
Тип публикации: Journal Article
Дата публикации: 2001-07-25
scimago Q1
wos Q1
БС1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5
ISSN: 15237060, 15237052
PubMed ID:
11506593
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
[reaction: see text]. Hydride reduction of C=N bonds stereocontrolled by intramolecular pi-stacking interactions of 1-naphthylsulfinyl and N-aryl groups, nonoxidative Pummerer rearrangement, and ring-closing metathesis are efficiently combined in a highly stereoselective entry to enantiomerically pure cyclic and acyclic fluorinated beta-amino alcohols and alpha-amino acid derivatives, respectively.
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ГОСТ
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Fustero S. et al. Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis: Intramolecular π-Stacking Interactions as a Source of Stereocontrol // Organic Letters. 2001. Vol. 3. No. 17. pp. 2621-2624.
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Fustero S., Navarro A., Pina B., Soler J. G., Bartolomé A., Asensio A., Simón A., Bravo P., Fronza G., Volonterio A., Zanda M. Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis: Intramolecular π-Stacking Interactions as a Source of Stereocontrol // Organic Letters. 2001. Vol. 3. No. 17. pp. 2621-2624.
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TY - JOUR
DO - 10.1021/ol016087q
UR - https://doi.org/10.1021/ol016087q
TI - Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis: Intramolecular π-Stacking Interactions as a Source of Stereocontrol
T2 - Organic Letters
AU - Fustero, Santos
AU - Navarro, Antonio
AU - Pina, Belén
AU - Soler, Juan García
AU - Bartolomé, Ana
AU - Asensio, Amparo
AU - Simón, Antonio
AU - Bravo, Pierfrancesco
AU - Fronza, Giovanni
AU - Volonterio, Alessandro
AU - Zanda, Matteo
PY - 2001
DA - 2001/07/25
PB - American Chemical Society (ACS)
SP - 2621-2624
IS - 17
VL - 3
PMID - 11506593
SN - 1523-7060
SN - 1523-7052
ER -
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BibTex (до 50 авторов)
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@article{2001_Fustero,
author = {Santos Fustero and Antonio Navarro and Belén Pina and Juan García Soler and Ana Bartolomé and Amparo Asensio and Antonio Simón and Pierfrancesco Bravo and Giovanni Fronza and Alessandro Volonterio and Matteo Zanda},
title = {Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis: Intramolecular π-Stacking Interactions as a Source of Stereocontrol},
journal = {Organic Letters},
year = {2001},
volume = {3},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/ol016087q},
number = {17},
pages = {2621--2624},
doi = {10.1021/ol016087q}
}
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MLA
Скопировать
Fustero, Santos, et al. “Enantioselective Synthesis of Fluorinated α-Amino Acids and Derivatives in Combination with Ring-Closing Metathesis: Intramolecular π-Stacking Interactions as a Source of Stereocontrol.” Organic Letters, vol. 3, no. 17, Jul. 2001, pp. 2621-2624. https://doi.org/10.1021/ol016087q.