6.4. Polyynes 3123 6.5. Using R-Hydroxy Stannanes 3124 6.6. Using the Hurtley Reaction 3124 6.7. Using a Methylenation Reaction 3125 7. Conclusions and Future Prospects 3125 8. Uncommon Abbreviations 3125 9. Acknowledgments 3125 10. Note Added in Proof 3125 11. References 3126 * Authorstowhomcorrespondenceshouldbeaddressed(evano@chimie.uvsq.fr, nicolas.blanchard@uha.fr). † Université de Versailles Saint Quentin en Yvelines. ‡ Université de Haute-Alsace. Chem. Rev. 2008, 108, 3054–3131 3054

Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis.

Organometallic chemistry on silicon and germanium surfaces.

https://www.chem.ccu.edu.tw/~joyce/referance/ericyang/Coord.%20Chem.%20Rev/Coord.%20Chem.%20Rev.%202004,%20248,%202337-2364.pdf

Copper in cross-coupling reactions: The post-Ullmann chemistry

http://aether.cmi.ua.ac.be/artikels/Artikels%20Gitte/Artikels/Reviews/Trans.%20Metal.%20catal.%20reactions%20Chem.%20rev.%20042127.pdf

Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis

The review covers the knowledge on photoremovable protecting
groups and includes all relevant chromophores studied in the
time period of 2000–2012; the most relevant earlier works are
also discussed.

/pdf/photoremovable-protecting-groups-in-chemistry-and-biology-2n33qs6p7b.pdf

Photoremovable Protecting Groups in Chemistry and Biology: Reaction Mechanisms and Efficacy

Recent advances in the chemistry of ynamines and ynamides

A copper-catalyzed new C−N bond formation involving a sp-hybridized carbon is described here leading to a facile entry for syntheses of chiral ynamides. This direct N-alkynylation of amides should have a significant impact on the future development of synthetic methodologies employing ynamides.

A copper-catalyzed C-N bond formation involving sp-hybridized carbons. A direct entry to chiral ynamides via N-alkynylation of amides.

Highly stereoselective synthesis of novel alpha-haloenamides via a mild and efficient hydrohalogenation of ynamides.

Monolayer assemblies on silicon surfaces are of interest for a number of technological reasons. Here, we present a novel, two-step strategy for assembly formation directly on silicon surfaces. In the first step, a H-terminated Si(100) or Si(111) surface reacts with Cl2 to give a Cl-capped surface. In the second step, the Cl−Si surface is immersed in an alcohol/isooctane solution for monolayer formation via Si−O linkages, with the removal of surface Cl likely in the form of HCl. This reaction mechanism is confirmed by X-ray photoelectron spectroscopy. X-ray reflectivity measurement shows that the thickness of the monolayer film is close to molecular dimension and the density is about 85% of that in crystalline paraffine. Fourier transform infrared spectroscopy and water contact angle measurements suggest that the alkyl chains within the monolayer possess, to a limited degree, conformational order. Atomic force microscopy image with molecular lattice resolution shows intermolecular distance corresponding to...

Molecular Assemblies on Silicon Surfaces via Si−O Linkages

The first successful base-promoted isomerization of propargyl amides to chiral ynamides. Applications in ring-closing metathesis of ene-ynamides and tandem RCM of diene-ynamides.

Jason A. Mulder

Papers

Recent advances in the chemistry of ynamines and ynamides

A copper-catalyzed C-N bond formation involving sp-hybridized carbons. A direct entry to chiral ynamides via N-alkynylation of amides.

Highly stereoselective synthesis of novel alpha-haloenamides via a mild and efficient hydrohalogenation of ynamides.

Molecular Assemblies on Silicon Surfaces via Si−O Linkages

The first successful base-promoted isomerization of propargyl amides to chiral ynamides. Applications in ring-closing metathesis of ene-ynamides and tandem RCM of diene-ynamides.