Low molecular weight synthetic peptides have been demonstrated to be effective catalysts
for an increasingly wide array of asymmetric transformations. In many cases, these peptide …

The advent of organocatalysis provided an additional option in every researcher's arsenal,
towards the development of elegant and sustainable protocols for various organic …

The Negishi cross-coupling is a powerful C–C bond-forming reaction widely utilised in many
areas of organic synthesis. This review details the use of Negishi cross-couplings in the …

Dioxiranes are multi-tasking reagents with mild and selective oxygen transfer attributes.
These oxidants are accessed from the reaction of ketones with an oxidant and are employed …

The area of fluorinated amino acid synthesis has seen rapid growth over the past decade.
As reports of singly fluorinated natural amino acid derivatives have grown, researchers have …

The enantioselective total synthesis of cage-shaped alkaloid (+)-arboridinine is reported.
The synthesis takes advantage of the stereoselective double-Mannich reaction to rapidly …

The aromatic core of an overcrowded alkene‐based molecular motor is extended with the
goal of inducing isomerization with visible light instead of harmful UV light. In our design, the …

A four-step procedure has been developed for the synthesis of (S)-3-isopropyl-1-[(R)-1-
phenylethyl)-1, 4-diazaspiro [4.5] decan-2-one with high diastereoselectivity (up to 95% de) …

Negishi cross-coupling reaction is a familiar reaction for the formation of carbon–carbon
bonds that couples organic halides or triflates with organozinc compounds. Palladium is …

The synthesis of chiral organic molecules is a purity‐driven research that has become an
essential part of our lives due to their applications in pharmaceuticals. Contemporary …