Correction: Professor (Dr) Sukh Dev: an iconic scientist with an innate sixth sense who radicalized natural product synthesis & organic chemistry
View abstract on PubMed
Summary
This summary is machine-generated.This correction clarifies details in a previous article honoring Professor Sukh Dev, a pivotal figure in natural product synthesis and organic chemistry. It ensures accurate representation of his significant scientific contributions.
Area Of Science
- Organic Chemistry
- Natural Product Synthesis
- Medicinal Chemistry
Context
- Professor Sukh Dev's seminal work has profoundly influenced organic chemistry.
- His research in natural product synthesis set new benchmarks in the field.
- This correction pertains to a previously published tribute article.
Purpose
- To amend and clarify specific information within the original article.
- To ensure the accurate portrayal of Professor Sukh Dev's scientific legacy.
- To maintain the integrity of scientific records in organic chemistry.
Summary
- The correction addresses minor inaccuracies in the tribute to Professor Sukh Dev.
- It reaffirms his status as a leading scientist in natural product synthesis.
- The article highlights his innovative approaches and impact on organic chemistry.
Impact
- Ensures the historical accuracy of Professor Sukh Dev's contributions.
- Provides a corrected reference for researchers in organic and medicinal chemistry.
- Upholds the standards of scientific communication and record-keeping.
Related Concept Videos
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
Kinetic Studies and Significance
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
Organic chemistry is the study of compounds of carbon called organic compounds. Organic compounds either originate from living organisms or are synthesized by chemists. A defining trait of these compounds is the presence of carbon as the principal element, which is bonded to other carbon atoms and other elements such as hydrogen, oxygen, nitrogen, and sulfur. The existence of a wide array of organic molecules is a consequence of carbon atoms’ ability to form up to four strong bonds to...
One of the critical aspects of the E1 reaction mechanism, as also observed in E2, is the regiochemistry, with multiple regioisomers obtained as products. In the example discussed, the presence of water as a weak base favors elimination over substitution to generate two alkenes. Given that alkenes’ stability increases with the number of alkyl groups across the double bond, typically, E1 reactions lead to the Zaitsev product, for this is more substituted and stable than the Hofmann product.

