Reaction 1: Synthesis of Citric Acid

Ferrocenecarboselenoic Acid: Synthesis and Some Reactions

Amino acid synthesis - Wikipedia

In most cases these amino acids can be synthesize by one step reactions from central metabolites. They are simple in structure and their synthesis is also straight forward.

Acid-mediated reactions under microfluidic conditions: A new strategy for practical synthesis of biofunctional natural products

Amino acid synthesis is the set of ..

The dihydroxylation-Petasis reaction method for enantioselective synthesis of 1,2-amino alcohols from vinyl sulfones has been applied to the synthesis of hyacinthacine B3. After formation of the α-hydroxyaldehyde, Petasis reaction with a chiral allylic amine and ()-β-styrenylboronic acid proceeded with moderate yield and high diastereoselectivity (Eq. 14).

The Strecker amino acid synthesis, devised by Adolph Strecker, is a series of chemical reactions that synthesize an amino acid from an aldehyde (or ketone).

In most cases bacteria would rather use amino acids in their environment than make them from scratch. It takes a considerable amount of energy to make the enzymes for the pathway as well as the energy required to drive some of the reactions of amino acid biosynthesis. The genes that code for amino acid synthesis enzymes and the enzymes themselves are under tight control and are only turned on when they are needed.

29/11/2006 · Hydrothermal Reactions of Pyruvic Acid: Synthesis, Selection, and Self-Assembly of Amphiphilic Molecules

Synthesis Reactions Lecture - YouTube

Alkynyl trifluoroborates are useful substrates for the synthesis of propargylic amines. Yield is highest when the solvent employed is the ionic liquid BmimBF4(1-butyl-3-methylimidazolium tetrafluoroborate), and secondary amines are required. One equivalent of benzoic acid may be required in reactions of salicylaldehydes (Eq. 11).

Synthesis and/or collection of amino acids is critical ..

A convergent total synthesis of (−)-nahuoic acid Ci(Bii) (3), a novel -decalin polyketide, has been achieved. Key synthetic transformations include Type II Anion Relay Chemistry (ARC) to construct the polyol chain, a Ti-catalyzed asymmetric Diels–Alder reaction to generate the -decalin skeleton, and a late-stage large fragment union exploiting a Micalizio alkoxide-directed alkyne–alkene coupling tactic.

General Chemistry/Types of chemical reactions - …

The biosynthesis of serine and glycine constitute a major metabolic pathway that plays a central role in the formation of other amino acids, nucleic acids and phospholipids. When is grown on glucose, fully 15% of carbon assimilated passes through the serine pathway. Synthesis of serine and glycine starts with oxidation of 3-phosphoglycerate forming 3-phosphohydroxy pyruvate and NADH. A transamination reaction with glutamate forms 3-phosphoserine and removal of the phosphate yields serine. Glycine is generated by removal of the methyl group from serine. Energy is not required for this pathway, in fact it yields energy in the form of reduced NADH.

Just as synthesis reactions can only form one ..

The synthesis of histidine is long and complex and its pathway is intertwined with nucleic acid biosynthesis (specifically purine). The pathway seems to be universal in all organisms able to synthesize histidine. The first five steps of the pathway take ribose from phosphoribosyl pyrophosphate (PRPP) and transform it into Imadiazoleglycerol phosphate. Once the imadiazole ring is formed, glutamate donates the -amino group and the newly formed amine is oxidized to histidine in the last step of the pathway. Energy is required in the form of ATP (in this case elements of the ATP molecule actually becomes part of the amino acid) and pyrophosphate which is lost from phosphoribosyl pyrophosphate and ATP help drive the reaction.

Acid-Base Reactions - Georgia State University

The fatty acid synthesis is initiated when holo-ACP, NADPH and NADH, acetyl-CoA and malonyl-CoA undergo condensation and subsequent reduction to form butyryl-ACP. These reactions are catalyzed by the malonyl-CoA:ACP transacylase FabD, the ketosynthase FabH, the NADPH-dependent ketoreductase FabG, either the dual-function dehydratase/isomerase FabA or the monofunctional dehydratase FabZ, and the NADH-dependent enoyl reductase FabI. Then the butyryl-ACP is extended via 5-7 rounds of analogous reactions to produce a C14 to C18-ACP either fully saturated or monounsaturated. These extension cycles are catalyzed by either the ketosynthase FabB or FabF in collaboration with FabD, FabG, FabA or FabZ, and FabI. Finally, the full-length fatty acid is released from the corresponding fatty acyl-ACP via hydrolysis by C16-specific thioesterase,TesA.