What is he best known for?
The fields of study he is best known for:
Marvin H. Caruthers focuses on Organic chemistry, Biochemistry, Combinatorial chemistry, Phosphoramidite and Oligonucleotide.
His Organic chemistry research includes themes of Nucleic acid and Nucleoside.
His Combinatorial chemistry study incorporates themes from Protein sequencing, Polymer, Gene, Chemical synthesis and Computational biology.
His Phosphoramidite research incorporates elements of Deoxyribonucleotide, Oligoribonucleotides and Oligonucleotide synthesis.
His Oligonucleotide research integrates issues from RNA, Molecular biology, Enzyme inhibitor and DNA synthesis.
His work in Polynucleotide addresses subjects such as Inorganic polymer, which are connected to disciplines such as Scientific method.
His most cited work include:
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis (1993 citations)
- Process for preparing polynucleotides (1385 citations)
- Improved free-energy parameters for predictions of RNA duplex stability (1197 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in DNA, Combinatorial chemistry, Biochemistry, Stereochemistry and Oligonucleotide.
The various areas that he examines in his DNA study include RNA, RNase H, Molecular biology, HeLa and Chemical synthesis.
His studies in Combinatorial chemistry integrate themes in fields like Nucleic acid, DNA synthesis, Nucleoside, Phosphoramidite and Organic chemistry.
His research integrates issues of Structural gene, Lac repressor, Duplex and Nucleotide in his study of Stereochemistry.
The concepts of his Nucleotide study are interwoven with issues in Binding site and Monomer.
His Oligonucleotide study combines topics from a wide range of disciplines, such as Phosphodiester bond, Nucleophile and Solid-phase synthesis.
He most often published in these fields:
- DNA (27.70%)
- Combinatorial chemistry (28.04%)
- Biochemistry (25.34%)
What were the highlights of his more recent work (between 2004-2020)?
- DNA (27.70%)
- Combinatorial chemistry (28.04%)
- Oligonucleotide (22.30%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in DNA, Combinatorial chemistry, Oligonucleotide, Organic chemistry and RNA.
His DNA study is concerned with Biochemistry in general.
Marvin H. Caruthers has included themes like Protecting group, Synthon, Polynucleotide, Nucleoside and Monomer in his Combinatorial chemistry study.
The Nucleoside study combines topics in areas such as Chemical synthesis, Nucleic acid and Moiety.
His Oligonucleotide study integrates concerns from other disciplines, such as Molecular biology, RNase P, Exon skipping and Stereochemistry.
His study in RNA is interdisciplinary in nature, drawing from both Complementary DNA, Transfection and Cell biology.
Between 2004 and 2020, his most popular works were:
- Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process (253 citations)
- Streamlined Process for the Chemical Synthesis of RNA Using 2′-O-Thionocarbamate-Protected Nucleoside Phosphoramidites in the Solid Phase (57 citations)
- Thiocarbon-protecting groups for rna synthesis (50 citations)
In his most recent research, the most cited papers focused on:
His main research concerns Combinatorial chemistry, Monomer, Polynucleotide, RNA and Nucleoside.
His Combinatorial chemistry research focuses on Phosphoramidite and how it connects with Chemical synthesis.
His work carried out in the field of Polynucleotide brings together such families of science as Nucleotide and Stereochemistry.
His study explores the link between RNA and topics such as DNA that cross with problems in Nanotechnology.
His study focuses on the intersection of Nucleoside and fields such as Nucleic acid with connections in the field of Organic chemistry, Aryl and Thiocarbonate.
In Thiocarbonate, Marvin H. Caruthers works on issues like Silylation, which are connected to Oligonucleotide.
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