Name Reaction List by Marcus Brackeen; MonomerChem Inc



Custom Synthesis & Medicinal Chemistry Area



Acyloin Condensation
Aldol Condensation
Arbuzov Reaction
Arndt-Eistert Synthesis
Baeyer-Villiger Reaction
Bamford-Stephens Reaction
Barbier Reactions
Barbier-Wieland Degradation
Barton Reaction
Barton-McCombie Reaction
Barton Olefin Synthesis
Baudisch Reaction
Baylis-Hillman Reaction
Bechamp Reduction
Beckmann Rearrangement
Beckmann Fragmentation
Benzilic Acid Rearrangement
Benzoin Condensation
Bergman Reaction
Bernthsen Acridine Synthesis
Biginelli Reaction
Birch Reduction
Bishler-Mohlau Indole Synthesis
Bishler-Napieralski Reaction
Blaise Reaction
Blanc Reaction
Bodroux Reaction
Borsche-Drechsel Cyclization
Brackeen Imidazole Synthesis
Brook Rearrangement
Bucherer-Bergs Reaction
Cannizzaro Reaction
Carroll Rearrangement
Castro-Stephens Coupling
Chichibabin Reaction
Claisen Condensation
Claisen Rearrangement
Clemmensen Reduction
Combes Quinoline Synthesis
Conrad-Limpach Reaction
Cope Rearrangement
Cope Elimination Reaction
Cory-Kim Oxidation
Craig Method
Curtius Rearrangement
Dakin Reaction
Dakin West Reaction
Darzens Condensation
Dess-Martin Oxidation
Dieckmann Reaction
Diels-Alder Reaction
Doebner Reaction
Edman Degradation
Einhorn -Brunner Reaction
Emmert Reaction
Ene Reaction
Eschenmoser Fragmentation
Favorskii Rearrangement
Feist-Benary Synthesis
Finkelstein Reaction
Fischer Indole Synthesis
Fischer Oxazole Synthesis
Flood Reaction
Friedel-Crafts Acylation
Friedel-Crafts Alkylation
Friedlander Synthesis
Fries Rearrangement
Gabriel Synthesis
Gattermann-Koch Reaction
Goldberg Reaction
Grob Fragmentation
Hammick Reaction
Harries Ozonide Reaction
Heck Reaction
Hell-Volhard-Zelinsky Reaction
Henry Reaction
Hinsberg Thiophene Synthesis
Hofmann Reaction
Hofmann-Martius Rearrangement
Horner-Emmons
Hunsdiecker Reaction
Jacobsen Epoxidation
Jones Oxidation
Knoevenagel Condensation
Knorr Pyrrole Synthesis
Knorr Quinoline Synthesis
Kolbe-Schmitt Reaction
Krapcho Decarboalkoxylation
Krohnke-Pyridine Synthesis
Kucherov Reaction
Leuckart Reaction
Letts Nitrile Synthesis
Lieben Iodoform Reaction
Lossen Rearrangement
Madelung Synthesis
Mannich Reaction
Milas Hydroxylation Reaction
Mitsunobu Reaction
McMurry Reaction
Meerwein-Ponndorf-Verley Reduction
Peterson Reaction
Pinner Reaction
Pfitzner-Moffatt Oxidation
Pictet-Gams Isoquinoline Synthesis
Pictet-Spengler Isoquinoline Synthesis
Piloty-Robinson Synthesis
Pinacol Rearrangement
Pomeranz-Fritsch Reaction
Polonovski Reaction
Quelet Reaction
Reformatski Reaction
Reissert Reaction
Reissert Indole Synthesis
Riehm Quinoline Synthesis
Riley Oxidation
Ritter Reaction
Robinson Annulation
Rosenmund Reduction
Rowe Rearrangement
Rubottom Oxidation
Ruff-Fenton Degradation
Sandmeyer Reaction
Scholl Reaction
Schmidt Rearrangement
Schotten-Baumann Reaction
Sharpless Dihydroxylation
Sharpless Epoxidation
Simmons-Smith Reaction
Simonis Chromone Cyclization
Skraup Reaction
Sommelet-Hauser Rearrangement
Stephen Aldehyde Synthesis
Stevens Rearrangement
Swern Oxidation
Tiemann Rearrangement
Ullmann Reaction
Wacker Oxidation
Wharton Reaction
Whiting Reaction
Wichterle Reaction
Wolff Rearrangement
Wolff Kishner Reduction
Wittig Reaction
1,2-Wittig Rearrangement
2,3- Wittig Rearrangement



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We perform inexpensive custom synthesis of complex organic compounds. The custom synthesis of organics can be performed by a variety of individuals. The cost however depends on how experienced the chemist actually is. If the chemist is a reproduction chemist and is attempting to veer away from an experimental protocol then the result will often be a bad custom synthesis operation. Promises of low cost for a custom synthesis is only a promise which can only be realized by the final delivery of the compound. We perform the custom synthesis of heterocycles, carbocycles, peptides, organic intermediates, Positron Emission Tomography intermediates and standards. We perform the custom synthesis of analytical reference standards and the custom synthesis of GMP starting materials. To perform a custom synthesis, many chemists require experimental protocols or references to the synthetic material in the past. We do not require any experimental reference material for any thermodynamically stable molecule in order to perform a custom synthesis. We conduct our own literature searches for a variety or organic transformations before quoting on a custom synthesis request so that we are highly confident that we can actually deliver a product on the quoted timeline. It may seem that outsourcing to asia in inexpensive at first; but much of the chemistry that we do here is optimization and creativity oriented custom synthesis work. Having years of experienced chemists and a wealth or knowledge with respect to problem solving skills in custom synthesis is what you get by interacting with monomerchem inc and custom synthesis inc. Imagine for example that you need the synthesis of a compound very similar to an existing drug but have no protocol for its custom synthesis. We routinely do this kind of work and we do it rapidly. We would rather generate an answer for our clients rather than a report full of excuses as to why the compound has not yet been produced. The custom synthesis of carbocycles and enantiopure or chiral compounds is also something that we routinely do. We begin by designing the synthesis of the enantiopure compound either by utilizing asymmetric synthesis or by a resolution technique; either way the compounds are delivered rapidly and efficiently. We perform the custom synthesis of heterocycles as well. The synthesis of a variety of heterocycles and a variety of chemically challenging compounds is routine work at monomerchem inc.