Results 131 to 140 of about 16,989 (195)
Some of the next articles are maybe not open access.
ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
M. lvarez, J. A. Joule
openaire +2 more sources
AbstractFor Abstract see ChemInform Abstract in Full Text.
M. lvarez, J. A. Joule
openaire +2 more sources
Enantioselective Hydrogenation of Isoquinolines
Angewandte Chemie International Edition, 2013Asymmetric hydrogenation of (hetero)arenes is one of the most straightforward ways to synthesize enantiomerically pure, saturated or partially saturated cyclic molecules. Recent progress has significantly expanded the substrate scope of this reaction.
Dongbing, Zhao, Frank, Glorius
openaire +2 more sources
Allylboration of Functionalized Isoquinolines.
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Fedor V Pastukhov +2 more
openaire +1 more source
THE SYNTHESIS OF SOME ISOQUINOLINES
Canadian Journal of Research, 1949A number of new isoquinolines substituted in the benzene nucleus have been prepared. The substituents include hydrazine-, chloro-, nitro-, and some combinations of these.
R H F, MANSKE, M, KULKA
openaire +2 more sources
1971
1. ISOQUINOLINE ALKALOIDS - ORIGINS AND DEGREDATION 2. ss-PHENYLETHYLAMINES AND SIMPLE ISOQUINOLINES 2.1 Structures 2.2 Syntheses 2.3 Chemical Properties 2.4 Polymeric Isoquinolines 2.5 N-Benzylisoquinolines 2.6 1-Phenylisoquinolines 2.7 4-Phenylisoquinolines 2.8 Biogenesis 2.9 Pharmacology References 3.
J. E. Saxton, K. W. Bentley
openaire +1 more source
1. ISOQUINOLINE ALKALOIDS - ORIGINS AND DEGREDATION 2. ss-PHENYLETHYLAMINES AND SIMPLE ISOQUINOLINES 2.1 Structures 2.2 Syntheses 2.3 Chemical Properties 2.4 Polymeric Isoquinolines 2.5 N-Benzylisoquinolines 2.6 1-Phenylisoquinolines 2.7 4-Phenylisoquinolines 2.8 Biogenesis 2.9 Pharmacology References 3.
J. E. Saxton, K. W. Bentley
openaire +1 more source
Hydrodenitrogenation of isoquinoline
Applied Catalysis A: General, 1999Abstract To determine the formation and reactivity of addition compounds produced during hydrodenitrogenation (HDN), we investigated the HDN of isoquinoline for a sulfided Ni–Mo/Al 2 O 3 catalyst operated under a hydrogen pressure of 12 MPa (cold charge) in the temperature range 300–375°C.
Yasuo Miki, Yoshikazu Sugimoto
openaire +1 more source
CXXII.—isoQuinoline and the isoquinoline-reds
J. Chem. Soc., Trans., 1922John Edmund Guy Harris +1 more
openaire +1 more source

