2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors.
about
Synthesis and biological evaluation of 3-(azolylmethyl)-1H-indoles and 3-(alpha-azolylbenzyl)-1H-indoles as selective aromatase inhibitors.Structure-activity relationships and docking studies of synthetic 2-arylindole derivatives determined with aromatase and quinone reductase 1.Design of Organic Transformations at Ambient Conditions: Our Sincere Efforts to the Cause of Green Chemistry Practice.Design for carbon–carbon bond forming reactions under ambient conditionsl-Proline catalyzed multicomponent one-pot synthesis of gem-diheteroarylmethane derivatives using facile grinding operation under solvent-free conditions at room temperatureOne-Pot Synthesis of 3-[(N-Alkylanilino)(aryl)methyl]indoles via a Transition Metal Assisted Three-Component Condensation at Room Temperature
P2860
2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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name
2- and 3-[
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2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors.
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type
label
2- and 3-[
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2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors.
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prefLabel
2- and 3-[
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2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors.
@en
P2093
P2860
P50
P1476
2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors
@en
P2093
Anja Palusczak
Guillaume Le Baut
Manuela Kogler
Marie-Pierre Lézé
Rolf W Hartmann
P2860
P304
P356
10.1080/14756360400004631
P577
2004-12-01T00:00:00Z