Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives
Тип публикации: Journal Article
Дата публикации: 1990-01-01
scimago Q2
wos Q2
БС2
SJR: 0.559
CiteScore: 4.6
Impact factor: 2.3
ISSN: 00397881, 1437210X
Catalysis
Organic Chemistry
Краткое описание
Derivatives of the title ring system are prepared in enantiomerically pure form from trans-4-hydroxy-L-proline . The target compounds are precursors of antibacterial quinolone carboxylic acids.
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Jordis U. et al. Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives // Synthesis. 1990. Vol. 1990. No. 10. pp. 925-930.
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Jordis U., Sauter F., Siddiqi S. M., Küenburg B., Bhattacharya K. Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives // Synthesis. 1990. Vol. 1990. No. 10. pp. 925-930.
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TY - JOUR
DO - 10.1055/s-1990-27056
UR - https://doi.org/10.1055/s-1990-27056
TI - Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives
T2 - Synthesis
AU - Jordis, Ulrich
AU - Sauter, Fritz
AU - Siddiqi, Suhaib M.
AU - Küenburg, Bernhard
AU - Bhattacharya, Kaberi
PY - 1990
DA - 1990/01/01
PB - Georg Thieme Verlag KG
SP - 925-930
IS - 10
VL - 1990
SN - 0039-7881
SN - 1437-210X
ER -
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@article{1990_Jordis,
author = {Ulrich Jordis and Fritz Sauter and Suhaib M. Siddiqi and Bernhard Küenburg and Kaberi Bhattacharya},
title = {Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives},
journal = {Synthesis},
year = {1990},
volume = {1990},
publisher = {Georg Thieme Verlag KG},
month = {jan},
url = {https://doi.org/10.1055/s-1990-27056},
number = {10},
pages = {925--930},
doi = {10.1055/s-1990-27056}
}
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MLA
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Jordis, Ulrich, et al. “Synthesis of (1R,4R)- and (1S,4S)-2,5-Diazabicyclo[2.2.1]heptanes and TheirN-Substituted Derivatives.” Synthesis, vol. 1990, no. 10, Jan. 1990, pp. 925-930. https://doi.org/10.1055/s-1990-27056.