Results
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[DOI: 10.1021/jm400138z]
Molecular structure and vibrational spectra of 4-, 5-, 6-chloroindole
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Structural Chemistry
[DOI: 10.1007/s11224-007-9247-x]
Joule, J. A., Science of Synthesis, (2001) 10, 489..
Dehydrogenation of 2,3-Dihydro-1H-indoles
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Science of Synthesis
Joule, J. A., Science of Synthesis, (2001) 10, 415..
From 2-(o-Aminoaryl)acetaldehydes
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Science of Synthesis
Joule, J. A., Science of Synthesis, (2001) 10, 438..
From o-(Chloroacetyl)arylamines; Sugasawa Synthesis
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Science of Synthesis
Fujita, Ken-ichi; Yamaguchi, Ryohei, Synlett 2005, 560-571.
Cp*Ir Complex-Catalyzed Hydrogen Transfer Reactions Directed toward Environmentally Benign Organic Synthesis
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Synlett
[DOI: 10.1055/s-2005-862381]
Friestad, G. K., Science of Synthesis, (2009) 40, 105..
Asymmetric Equivalents of the Tscherniac–Einhorn Reaction
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Science of Synthesis
Nakao, Y., Science of Synthesis: Catalytic Transformations via C?H Activation, (2015) 1, 367..
Arylation with Aryl Electrophiles/Nucleophiles
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Science of Synthesis
Nakao, Y., Science of Synthesis: Catalytic Transformations via C?H Activation, (2015) 1, 407..
Arylation with Hetarenes: Homocoupling of Hetarenes
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Science of Synthesis
Ipaktschi, J.; Saidi, M. R., Science of Synthesis Knowledge Updates, (2012) 4, 417..
Iron-Catalyzed Cross-Dehydrogenative Coupling Reactions of -Butoxycarbonyl-Protected 1,2,3,4-Tetrahydroisoquinoline and Indoles
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Science of Synthesis
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