4.4. Pd on Modified Silica 159 4.5. Pd on Clay and Other Inorganic Materials 159 5. Stille, Fukuyama, and Negishi Reactions 159 5.1. Stille Reactions 159 5.1.1. Pd on Carbon (Pd/C) 159 5.1.2. Palladium on KF/Al2O3 159 5.1.3. Pd on Modified Silica (SiO2/TEG/Pd) 159 5.2. Fukuyama Reactions 159 5.2.1. Pd on Carbon (Pd/C) 159 5.2.2. Pd(OH)2 on Carbon (Perlman’s Catalyst) 160 5.3. Pd/C-Catalyzed Negishi Reactions 160 6. Ullmann-Type Coupling Reactions 161 6.1. Pd/C-Catalyzed Aryl−Aryl Coupling 161 6.2. Pd/C-Catalyzed Homocoupling of Vinyl Halides 162

https://www.chem.ccu.edu.tw/~joyce/referance/ericyang/Chem.%20Rev/Chem.%20Rev.%202007,%20107,%20133-173.pdf

Carbon-Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts

Practical methodologies for the synthesis of indoles.

A surface science perspective on TiO2 photocatalysis

Since the discovery of organic azides by Peter Griess more than 140 years ago, numerous syntheses of these energy-rich molecules have been developed. In more recent times in particular, completely new perspectives have been developed for their use in peptide chemistry, combinatorial chemistry, and heterocyclic synthesis. Organic azides have assumed an important position at the interface between chemistry, biology, medicine, and materials science. In this Review, the fundamental characteristics of azide chemistry and current developments are presented. The focus will be placed on cycloadditions (Huisgen reaction), aza ylide chemistry, and the synthesis of heterocycles. Further reactions such as the aza-Wittig reaction, the Sundberg rearrangement, the Staudinger ligation, the Boyer and Boyer-Aube rearrangements, the Curtius rearrangement, the Schmidt rearrangement, and the Hemetsberger rearrangement bear witness to the versatility of modern azide chemistry.

Organic Azides: An Exploding Diversity of a Unique Class of Compounds

https://chemistry.mdma.ch/hiveboard/rhodium/pdf/archive/merbst/quinoline1999.pdf

Quinoline, quinazoline and acridone alkaloids

Microbial hydroxylation of heteroyohimbine alkaloids

Combined size-exclusion—ion-exchange high-performance liquid chromatographic analysis of parietaria pollen extracts with the aid of isoelectrofocusing and radio-allergo-sorbent test

Stefano Tollari

Papers

Microbial hydroxylation of heteroyohimbine alkaloids

Combined size-exclusion—ion-exchange high-performance liquid chromatographic analysis of parietaria pollen extracts with the aid of isoelectrofocusing and radio-allergo-sorbent test

Catalytic oxidation of benzylic amines to imines by M(TPP)CL (M = Fe, Mn) followed by reduction to secondary amines

A One-pot Synthesis of 2,6,7,12-Tetrahydroindolo[2,3-a]-quinolizin-4 (3H)-ones

Analysis of allergenic components of a parietaria judaica pollen extract by chromatographic methods for the evaluation of purification procedures