Relevant bibliographies by topics / Organic Synthessis

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Organic Synthessis'

Author: Grafiati
Published: 20 July 2024
Last updated: 31 July 2025

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Journal articles on the topic "Organic Synthessis"

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Dai, Mingji, Xinpei Cai, and Yu Bai. "Total Syntheses of Spinosyn A." Synlett 29, no. 20 (2018): 2623–32. http://dx.doi.org/10.1055/s-0037-1610249.

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Spinosyn A is an important polycyclic natural product with impressive insecticidal activity and has been used worldwide in agriculture as the major component of Spinosad. Herein, four chemical total syntheses of spinosyn A are summarized. Its biosynthesis and a chemoenzymatic total synthesis are discussed as well.1 Biosynthesis2 The Evans Synthesis3 The Paquette Synthesis4 The Roush Synthesis5 The Liu Synthesis6 The Dai Synthesis7 Conclusions
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Trofimov, B. A., and E. Yu Schmidt. "SUPERBASES IN ORGANIC SYNTHESIS." Chemical Problems 20, no. 4 (2022): 325–40. http://dx.doi.org/10.32737/2221-8688-2022-3-325-340.

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In this concise review, an emphasis is laid on the important role of superbases as catalysts and reagents in organic synthesis that so far remain underestimated. Diverse approaches to understand the superbasicity phenomenon are considered and the definition of superbase is given. Typical compositions of most widespread superbase systems are systematized and tabulated. The representative classic organic reactions assisted by superbases are surveyed.
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Huang, Jianhui, Caifeng Li, Liu Liu, and Xuegang Fu. "Norbornene in Organic Synthesis." Synthesis 50, no. 15 (2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.

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The norbornene skeleton possesses an alkene functionality with a fixed conformation, and represents unique reactivity. The use of norbornene and analogues as substrates is overviewed; reactivities are discussed as well as the role of norbornenes as ligands assisting modern organic transformations.1 Introduction2 Synthesis of Substituted Norbornenes2.1 Preparation of Functionalized Norbornenes by Deprotonation and Substitution Reactions2.2 Preparation of Functionalized Norbornenes under Palladium-Catalyzed­ Reaction Conditions2.3 Alkylation of Norbornene2.4 Multistep Synthesis3 Synthesis of Sub
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Fang, Zhang, and Yu Yang. "Research Progress of Application of Porous Polymer in Energy Storage." Advanced Materials Research 621 (December 2012): 27–30. http://dx.doi.org/10.4028/www.scientific.net/amr.621.27.

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Nowadays, one of the research emphases in clean energy field is to apply porous polymer as energy storage media to capture and save abundant energy. Researches in this area focus on theoretical methods and syntheses of new materials. Researches on theoretical methods include investigations on mechanical strength, characteristic of heat and mass transfer, internal structure and hydrophilicity of materials using mathematical, physical and chemical methods. Syntheses of new materials include synthesis of porous carbon and porous metal organic frameworks materials and construction of battery struc
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Tatrishvili, Tamara, and Omar Mukbaniani. "Cyclic Silicon Organic Copolymers: Synthesis and Investigation. Review." Chemistry & Chemical Technology 18, no. 2 (2024): 131–42. http://dx.doi.org/10.23939/chcht18.02.131.

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This paper considers the synthesis and investigation of cyclic silicon-organic polymers with mono- and polycyclic fragments in the side chain. For obtaining monocyclic polymers, the hydrosilylation reaction of 1-hydro-3-vinylhexamethylcyclotetrasiloxane was used. The reaction was conducted in a CCl4 solution at 75°C in the presence of Speier’s catalyst (H2PtCl6  6H2O) to produce a viscous-flow at room temperature polymer. The polymers were studied by NMR spectroscopy. Poly(carbosiloxane) with cyclic fragments in the methyl-siloxane backbone was synthesized by the hydride polyaddition of divin
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Chabukswar, Vasant, Sanjay Bhavsar, and Amit Horne. "Organic Synthesis and Characterization of Electrically Conducting Poly(o-Toluidine) Doped with Organic Acid." Chemistry & Chemical Technology 5, no. 1 (2011): 37–40. http://dx.doi.org/10.23939/chcht05.01.037.

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Yevchuk, Iryna, Oksana Demchyna, Viktoriya Kochubey, Hanna Romaniuk, and Zenoviya Koval. "Synthesis and Characterization of Organic-Inorganic Membranes Containing Sulphogroups." Chemistry & Chemical Technology 7, no. 1 (2013): 89–93. http://dx.doi.org/10.23939/chcht07.01.089.

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Sharma, Upendra, Inder Kumar, and Rakesh Kumar. "Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization." Synthesis 50, no. 14 (2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.

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Indole is an important heterocyclic motif that occurs ubiquitously in bioactive natural products and pharmaceuticals. Immense efforts have been devoted to the synthesis of indoles starting from the Fisher indole synthesis to the recently developed C–H activation/functionalization-based methods. Herein, we have reviewed the progress made on the regioselective synthesis of functionalized indoles, including 2-substituted, 3-substituted and 2,3-disusbstituted indoles, since the year 2010.1 Introduction2 Metal-Catalyzed Synthesis of 2-Substituted Indoles3 Metal-Catalyzed Synthesis of 3-Substituted
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Wang, Yi, Han Ding, and Ge Ging Xu. "Computer Aided Organic Synthesis Based on Graph Grammars." Applied Mechanics and Materials 411-414 (September 2013): 227–30. http://dx.doi.org/10.4028/www.scientific.net/amm.411-414.227.

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Traditionally, computer aided organic synthesis is based on the one-dimensional string model that employs string grammars to tackle the structure of molecular; the processing of organic reactions, and the establishment of the knowledge bases and file systems. Because of the limitations of one-dimensional method for tackling two-dimensional issues like organic syntheses, this paper presents a method for computer aided organic synthesis based on two-dimensional graph grammars. The method could apply the basic principle of the graph grammars to effectively and efficiently solve organic synthesis
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Liu, Can, Weiming Xu, Zongbin Zhang, et al. "The Potential for Organic Synthesis in the Ocean of Enceladus." Astrophysical Journal 971, no. 1 (2024): 51. http://dx.doi.org/10.3847/1538-4357/ad534f.

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Abstract The Cassini spacecraft detected a soup of organics in the plume of Saturn’s moon Enceladus. Those compounds could provide building blocks for the potential emergence or sustenance of microbial life in Enceladus’ subsurface ocean. However, the sources and stabilities of organics in Enceladus’ ocean are still poorly understood. Here, we perform nonequilibrium thermodynamic calculations to assess the energetics of abiotic synthesis for a broad spectrum of small organic molecules under both cold oceanic and hydrothermal conditions on Enceladus. Most of the organics that we studied are the
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Dissertations / Theses on the topic "Organic Synthessis"

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Paradis, Michel 1976. "The design and synthessis of platinum-based DNA intercalators /." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=31523.

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Over the past years, considerable attention has focused on the synthesis of small complexes that can bind and react at specific DNA sequences. This understanding of how to target DNA sites with specificity becomes important for nucleotide probing and novel chemotherapeutics.<br>Inert and stable transition-metal complexes are already being used for this purpose. Square planar platinum (II) complexes containing an aromatic heterocyclic ligand can insert and stack between the double helix base pairs. Two known ligands, DPPZ and phi, do intercalate DNA when chelating ruthenium, rhodium, or osmium.
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Phung, Bich Tuyen. "Etude de la sélectivité dans la réaction de Buchner." Electronic Thesis or Diss., Université Grenoble Alpes, 2024. https://theses.hal.science/tel-04651531.

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Le travail présenté dans ce manuscrit est divisé en deux grandes parties. Dans un premier temps, une étude sera présentée sur des problème de chimiosélectivité observés lors de la réaction de transfert de carbène. Des composés diazo différemment substitués ont été généré comme précurseur de carbène, et la réaction de transfert de carbène a été effectuée en présence de Rh2(OAc)4. Les résultats montrent une compétition entre la réaction de Buchner et l’insertion C‒H en position benzylique, dépendant de la substituant du diazo. Des calculs de DFT ont ensuite été réalisés pour compléter les inform
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Trupina, Snjezana. "Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases." Thesis, Linköping University, Linköping University, Organic Chemistry, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-57989.

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<p>Abnormal aggregation of misfolded proteins is related to numerous neurodegenerative diseases, which include Alzheimer’s, Parkinson’s disease and prion diseases. Luminescent conjugated probes (LCPs) have been used as dyes for these supramolecular assemblies termed amyloid fibrils. To these probes, metalloporphyrin (MP) derivates have been attached to achieve new spectroscopic properties, which will allow for new ways to study protein aggregation diseases.</p><p>In this thesis the synthesis of two different LCPs anchored porphyrin derivates are described. The LCPs are synthesized from 3-thiop
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Tilliet, Mélanie. "Synthesis and study of new oxazoline-based ligands." Doctoral thesis, KTH, Organisk kemi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4858.

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This thesis deals with the study of oxazoline-based ligands in metal-catalyzed asymmetric reactions. The first part describes the synthesis of six new bifunctinal pyridine-bis(oxazoline) ligands and their applications in asymmetric metal-catalysis. These ligands, in addition to a Lewis acid coordination site, are equipped with a Lewis basic part in the 4-position of the oxazoline rings. Dual activation by means of this system was probed in cyanide addition to aldehydes. The second part is concerned with the synthesis of two pyridine-bis(oxazoline) ligands bearing bulky triazole groups in the 4
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Winberg, Karl Johan. "Carborane Derivatives for Nuclide Therapy and Imaging : Synthesis and Radio-labelling." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ-bibl. [distributör], 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3561.

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Fyrner, Timmy. "Synthesis of Structures Related to Antifreeze Glycoproteins." Thesis, Linköping University, The Department of Physics, Chemistry and Biology, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-11941.

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<p>In this thesis, synthesis of structures related to antifreeze glycoproteins (AFGPs) are presented. Synthetic routes to a protected carbohydrate derivative, 2,3,4,6-tetra-O-benzyl-β-galactopyranosyl-(1→3)-2-deoxy-2-azido-4,6-di-O-benzyl-β-D-thio-1-galactopyranoside, and a tBu-Ala-Thr-Ala-Fmoc tripeptide, are described. These compounds are meant to be used in the assembly of AFGPs and analogues thereof. A Gal-GlcN disaccharide was synthesized via glycosylation between the donor, bromo-2-O-benzoyl-3,4,6-tri-O-benzyl-α-Dgalactopyranoside, and acceptor, ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthal
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Larsson, Andreas. "Synthesis, structure and conformation of oligo- and polysaccharides." Doctoral thesis, Stockholm University, Department of Organic Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-172.

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<p>Carbohydrates are a complex group of biomolecules with a high structural diversity. Their almost omnipresent occurrence has generated a broad field of research in both biology and chemistry. This thesis focuses on three different aspects of carbohydrate chemistry, synthesis, structure elucidation and the conformational analysis of carbohydrates.</p><p>The first paper describes the synthesis of a penta- and a tetrasaccharide related to the highly branched capsular polysaccharide from <i>Streptococcus pneumoniae </i>type 37. In the second paper, the structure of the O-antigenic repeating unit
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Esfandiarfard, Keyhan. "Novel Organophosphorus Compounds for Materials and Organic Synthesis." Doctoral thesis, Uppsala universitet, Molekylär biomimetik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-328295.

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This thesis is devoted to the development of new organophosphorus compounds for potential uses in material science and as reagents in Organic Chemistry. Organophosphorus compounds in a single molecule or organic electronics context are appealing as the phosphorous centers perturb the electronic properties of the π-conjugated systems while at the same time provide synthetic handles for subsequent synthetic modifications. As such, new synthetic methodology to such compounds and the exploration of new building blocks is of considerable interest. In a different study, novel organophosphorus compou
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BERTON, GIACOMO. "SYNTHESIS OF TRIPHENYLENES FOR SUPRAMOLECULAR APPLICATIONS." Doctoral thesis, Università degli Studi di Trieste, 2020. http://hdl.handle.net/11368/2969361.

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In this Doctoral Thesis, through several examples of new chemical modifications characterized by high yields and selectivities and new supramolecular structures, held together by a wide range of intermolecular forces forming several new host systems, we reached our target to revamp triphenylene and derivatives as a new molecular scaffold in supramolecular chemistry. More specifically, the introduction in our triphenylenic scaffold of alkyl thiol chains allowed the formation of sulphide and disulphide covalent cages, while by insertion of pyridine moieties through Mannich reaction it was possib
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Hagberg, Daniel. "Synthesis of Organic Chromophores for Dye Sensitized Solar Cells." Licentiate thesis, Stockholm : Kemi, Kungliga Tekniska högskolan, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4600.

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Books on the topic "Organic Synthessis"

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Hans-Günther, Schmalz, and Wirth Thomas 1964-, eds. Organic synthesis highlights V. Wiley-VCH, 2003.

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Volke, J. Electrochemistry in organic synthesis. Springer-Verlag, 1994.

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Taber, Douglass F. Organic Synthesis. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.

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Smith, Michael B. Organic synthesis. McGraw-Hill, 1994.

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Willis, Christine L. Organic synthesis. Oxford University Press, 1995.

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Smit, W. A. Organic synthesis: The science behind the art. Royal Society of Chemistry, 1998.

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Ho, Tse-Lok. Stereoselectivity in synthesis. Wiley, 1999.

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Svoboda, Jiří. Organická syntéza I. Vysoká škola chemicko-technologická, 2000.

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M, Trost Barry, and International Union of Pure and Applied Chemistry., eds. Stereocontrolled organic synthesis. Blackwell Scientific Publications, 1994.

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Protti, Stefano, and Alessandro Palmieri, eds. Sustainable Organic Synthesis. Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164842.

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Book chapters on the topic "Organic Synthessis"

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Yamada, Shinji. "Organic Synthesis". У The Cation–π Interaction. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-7335-2_4.

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Ameta, Chetna, Arpit Kumar Pathak, and P. B. Punjabi. "Organic Synthesis." In Sonochemistry. Apple Academic Press, 2018. http://dx.doi.org/10.1201/b22323-4.

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Okuyama, Tadashi, and Howard Maskill. "Organic Synthesis." In Organic Chemistry. Oxford University Press, 2013. http://dx.doi.org/10.1093/hesc/9780199693276.003.0023.

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This chapter looks at the reactions used in organic synthesis. It defines organic synthesis as the directed preparation of a sought compound usually, but not invariably, with some structural complexity from simple, readily available compounds. The chapter also develops the concept of retrosynthesis further and examines how to identify routes for syntheses of target compounds by applying organic reactions. Organic synthesis is one of the ultimate goals of organic chemistry and provides limitless opportunities to challenge the scientific imagination. The chapter then proceeds to discuss the synt
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Willis, Christine L., and Martin Wills. "Selected organic syntheses." In Organic Synthesis. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557913.003.0008.

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This chapter presents a case history of selected syntheses of a class of natural products known as the pyrrolizidine alkaloids to bring together the aspects of organic synthesis. The pyrrolizidines are a group of alkaloids which are characterized by the presence of the basic necine skeleton. The pyrrolizidine alkaloids exhibit remarkably diverse types of biological activity and have been reported to act as antitumor agents. The chapter then describes four methods for the synthesis of the pyrrolizidine alkaloids. Each route has its own particular merits, e.g. the route to platynecine gives the
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"Alkyne Metathesis in Synthesis: Syntheses of (+)-Ferrugine and Anatoxin-α." In Organic Synthesis. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.ch42.

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Morrow, Gary W. "Brief Organic Review." In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0004.

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In addition to simple hydrocarbon structures (alkanes, alkenes, alkynes, and aromatic systems) and alkyl groups (methyl, ethyl, propyl, isopropyl, etc.), this text assumes a familiarity with the most common functional groups associated with organic chemical structures and their basic reactivity patterns. Table 1.1 summarizes the names and structures of some of the more important functional groups we will be dealing with throughout the remainder of the book. It is important to remember that functional groups containing O or N with nonbonding electrons have an affinity for both protic and Lewis
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Smith, Michael B. "Retrosynthesis, Stereochemistry, and Conformations." In Organic Synthesis. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00001-5.

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Smith, Michael B. "Acids, Bases, and Addition Reactions." In Organic Synthesis. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00002-7.

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Smith, Michael B. "Functional Group Exchange Reactions." In Organic Synthesis. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00003-9.

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Smith, Michael B. "Acids, Bases, and Functional Group Exchange Reactions." In Organic Synthesis. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00004-0.

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Conference papers on the topic "Organic Synthessis"

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Smith, Warren E., William J. Dallas, Heidi A. Schlitt, and Walter Kullmann. "Reconstructing a Vector Current Distribution from its Magnetic Field Using Linear Estimation Theory." In Signal Recovery and Synthesis. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/srs.1986.wa2.

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Several methods currently exist for exploring the three-dimensional structure of the organs of the human body. They include x-ray computed tomography (CT),1 magnetic resonance imaging (MRI),2 and emission computed tomography (ECT).3,4 These techniques provide spatial information about an organ's attenuation coefficient, proton density, or the ability of the organ to take up a radioactive pharmaceutical, respectively.
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Barbosa, Alexandre F., and Arlene G. Corrêa. "Synthesis of 9-substituted 9-deazaguanine derivatives." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0125-2.

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Araujo, Yara J. K., Isac G. Rosset, and André L. M. Porto. "A New Synthesis of Benzonitriles Catalyzed by Microwave Irradiation." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0003-1.

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Rosset, Isac G., and André L. M. Porto. "Transesterification and Quantification by 1H NMR of Triester Oleate by Candida antarctica Lipase." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0004-1.

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da Silva, A. J. M., C. Schneider, and V. Snieckus. "Construction of Polyarylated Fluorenones via chemoselective Ru- and Pd-Catalyzed Suzuki Cross-Coupling Reactions." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0007-1.

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Andrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins, and Nilo Zanatta. "Highly Efficient Synthesis of CF3-Containing 7-Aminoquinolines From Cyclocondensation Reaction of Trifluoroacetyl Enamine Precursors." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0008-1.

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Andrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins, and Nilo Zanatta. "General Pathway for One-Pot Synthesis of Trifluoromethyl- Containing 2-Amino-cycloalka[b][1,8]naphthyridines." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0008-2.

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Navarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, et al. "Synthesis of New 5-Trifluoromethyl-3-alkyl[aryl(heteroaryl)]-4- (2-benzyl-3-hydroxycyclohex-2-enone-2-yl)-1H-pyrazoles by a Ring-Opening Reaction." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-1.

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Navarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Marcos A. P. Martins, and Nilo Zanatta. "Molecular Iodine - An Efficient Oxidative Reagent for Aromatization of Trifluoromethyl Substituted Chromenones." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-2.

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Rampon, Daniel S., Aloir A. Merlo, and Paulo H. Schneider. "Synthesis of New Liquid-Crystalline Selenophenes via Electrophilic Cyclization of (Z)-Selenoenynes." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0011-1.

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Reports on the topic "Organic Synthessis"

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Reilly, S. D., D. R. Click, S. K. Grumbine, B. L. Scott, and J. G. Watkins. Asymmetric catalysis in organic synthesis. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/677032.

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Rittman, Bruce. Biotic Transformations of Organic Contaminants. The Groundwater Project, 2023. http://dx.doi.org/10.21083/ousn4116.

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Biodegradation—the breakdown of organic matter by microorganisms—is an important groundwater process that occurs naturally and is especially important for the in situ cleanup of contaminated groundwater. Pollutant biodegradation follows well-established principles that are summarized in this book. The first principle is that the microorganisms must grow and sustain themselves by oxidizing an electron-donor substrate (food) and transferring the electrons to an electron-acceptor substrate (respiration). This electron flow generates energy that the microorganisms use to fuel biomass synthesis. Mo
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Liu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/897369.

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Bernstein, J., J. Y. Becker, S. Bittner, and S. S. Shaik. Electrically Conducting Organic Materials: Design, Synthesis and Characterization. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada195095.

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Folz, Katherine E. Synthesis and Characterization of Novel Organic Conducting Polymers. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada425003.

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Ramírez, David A., Cecilia Silva-Díaz, Johan Ninanya, et al. Potato zero-tillage and mulching is promising in achieving agronomic gain in Asia. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.6.0072.

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Review question / Objective: The objective of this review is to analyze the effect of zero-tillage and organic mulching (with emphasis on rice-straw) on several Key Performance Indicators (KPIs) related to productivity, resources-use efficiency, and soil health, as well as, C footprint, and weed control for growing potatoes in rice-based systems in Asia. Can zero-tillage and organic mulching increase agronomic gain in potatoes crop in Asia? Rationale: Potato cultivation under zero-tillage and mulching (PZTM) between rice or rice-other crops projects a sustainable intensification of rice-based
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Belfort, Georges. Combinatorial Membrane Synthesis: Fundamentals of Hybrid Metal-Organic Brush (MOB) Membranes for Organic Solvent Nanofiltration (Renewal). Office of Scientific and Technical Information (OSTI), 2024. https://doi.org/10.2172/2335921.

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Zhang, Honghu. Bioinspired synthesis and self-assembly of hybrid organic–inorganic nanomaterials. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1409201.

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Singh, Anjali. Amino Acids: Building Blocks of Proteins. ConductScience, 2022. http://dx.doi.org/10.55157/cs20220612.

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Abstract:
Amino acids are essential organic compounds serving as protein building blocks. Recognized for their biological roles, they underpin proteins' structure and interactions. Classified by polarity and nutritional necessity, essential amino acids, not synthesized by the body, include histidine, leucine, lysine, and more, while non-essential ones are produced internally. These molecules exhibit diverse functions, from neurotransmitter precursor synthesis to immune support. Industries leverage amino acids in animal feed, artificial sweeteners, flavor enhancers, and drug manufacturing, highlighting t
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Sun, Ning. Process scale-up and optimization of the metal-organic framework synthesis. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1618846.

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