المؤلفون: Sridhar Musulla, Bharathi Y Kumari, Srinivasa A Rao

المصدر: International Research Journal Of Pharmacy. 9:161-164

مصطلحات موضوعية: Chemistry, Total synthesis, Organic chemistry, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::44e1ca690df793fcb5ceb17f2d776c55
https://doi.org/10.7897/2230-8407.099206

المؤلفون: Choragudi Chandrasekhar, Rudraraju Ramesh Raju, Reddymasu Sreenivasulu, Gurrala Alluraiah

المصدر: Natural Product Research. 33:2738-2743

مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Hydrolysis, Organic Chemistry, Total synthesis, Stereoisomerism, Plant Science, Ketones, 01 natural sciences, Biochemistry, 0104 chemical sciences, Analytical Chemistry, Kinetic resolution, 010404 medicinal & biomolecular chemistry, Cyclization, Heterocyclic Compounds, Wittig reaction, Swern oxidation, Epoxy Compounds, Organic chemistry, Stereoselectivity, Oxidation-Reduction, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbb90db26448e2977285d5b2ab740582
https://doi.org/10.1080/14786419.2018.1499636

المؤلفون: David R. McMullin, Grace Daly, Hai D. T. Nguyen, J. D. Miller, B.S. Menard

المصدر: Fungal Ecology. 31:1-8

مصطلحات موضوعية: 0301 basic medicine, Ecology, biology, Ecological Modeling, fungi, Plant Science, Griseofulvin, biology.organism_classification, Endophyte, Pinus , Choristoneura fumiferana, 03 medical and health sciences, chemistry.chemical_compound, 030104 developmental biology, chemistry, Seedling, Vermiculine, Cronartium ribicola, Botany, Ecology, Evolution, Behavior and Systematics, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fa70c531088ea36a52a6f2b2d70a5307
https://doi.org/10.1016/j.funeco.2017.09.003

المؤلفون: Naresh Kumar Vuppula, Dongamanti Ashok, Sridhar Pervaram, Sreenivasulu Reddymasu, Venkata Ramana Reddy Chittireddy

المصدر: Chemical Papers. 72:971-977

مصطلحات موضوعية: 010405 organic chemistry, Chemistry, General Chemical Engineering, Convergent synthesis, Total synthesis, General Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Combinatorial chemistry, Industrial and Manufacturing Engineering, 0104 chemical sciences, Yield (chemistry), Materials Chemistry, Stereoselectivity, Mitsunobu reaction, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3c25353e111ab4798db60414ebb5d891
https://doi.org/10.1007/s11696-017-0331-4

المؤلفون: A. Venkat Narsaiah, G. Nagalatha, Siva Ganesh Narala

مصطلحات موضوعية: 010405 organic chemistry, Pinnick oxidation, Organic Chemistry, Epoxide, Regioselectivity, Total synthesis, Plant Science, 01 natural sciences, Biochemistry, 0104 chemical sciences, Analytical Chemistry, 010404 medicinal & biomolecular chemistry, chemistry.chemical_compound, chemistry, Organic chemistry, Stereoselectivity, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e675d4e591d7e8c00925b32660f1c8

المؤلفون: Dejan Orčić, Jasna Mastilović, Elizabet Janić Hajnal

مصطلحات موضوعية: biology, Alternariol, food and beverages, Alternaria, biology.organism_classification, chemistry.chemical_compound, chemistry, Genus, Tentoxin, Botany, otorhinolaryngologic diseases, Macrosporin, Tenuazonic acid, Alterperylenol, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b6acb8b8e8b205fa5a46ee15a78b614d
https://doi.org/10.1016/b978-0-12-814639-2.00004-6

المؤلفون: Barreddi Chiranjeevi, Reddymasu Sreenivasulu, Vuppula Naresh Kumar, Perugu Edukondalu, Rudraraju Ramesh Raju

المصدر: Monatshefte für Chemie - Chemical Monthly. 146:1309-1314

مصطلحات موضوعية: Hydrolysis, chemistry.chemical_compound, chemistry, Intermolecular force, Oxide, Total synthesis, Organic chemistry, Stereoselectivity, General Chemistry, Propylene oxide, Kinetic resolution, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8e228010a679d34023ec4a70832d26f8
https://doi.org/10.1007/s00706-014-1406-3

المؤلفون: Sumarah, M.W. (Mark W.), Walker, A.K. (Allison K.), Seifert, K.A. (Keith A.), Todorov, A. (Adrian), Miller, JD (J. David)

مصطلحات موضوعية: Lophodermium, Needle endophytes, Pyrenophorol, White pine, White pine blister rust

Relation: https://ir.library.carleton.ca/pub/13949

الاتاحة: https://ir.library.carleton.ca/pub/13949
https://doi.org/10.1007/978-3-319-20397-3_8

المؤلفون: Saroja Nuguri, Laxminarayana Eppakayala, Naresh Kumar Vuppula, Prasad Kottapalli Rajasekhara

المصدر: Journal of Pharmacy Research. 7:559-564

مصطلحات موضوعية: Sharpless epoxidation, Hydrolysis, Chemistry, Stereochemistry, Organic chemistry, Total synthesis, Mitsunobu reaction, Enantiomer, Reductive elimination, Kinetic resolution, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d8722c31d44e19f5145adf8c69698b50
https://doi.org/10.1016/j.jopr.2013.06.006

المؤلفون: Ahmad Al Khazim Al Ghamdi, Jhillu S. Yadav, Tenneti Srinivasa Rao, Ganapuram Madhusudhan Reddy, Basi V. Subba Reddy

المصدر: Synthesis. 44:783-787

مصطلحات موضوعية: Chemistry, Organic Chemistry, Total synthesis, Organic chemistry, Stereoselectivity, Photochemistry, Catalysis, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::06df8b1969fbee0d21dfa47cb10c0aa6
https://doi.org/10.1055/s-0031-1289703

المؤلفون: Ulrich Flörke, Umar Farooq, Gennaro Pescitelli, Tibor Kurtán, Karsten Krohn, Sándor Antus, Piero Salvadori, Siegfried Draeger, Barbara Schulz

المصدر: European Journal of Organic Chemistry. 2007:3206-3211

مصطلحات موضوعية: Antifungal, biology, Chemistry, Stereochemistry, medicine.drug_class, Organic Chemistry, Absolute configuration, Solid-state, Time-dependent density functional theory, biology.organism_classification, Természettudományok, Synonym (taxonomy), Phoma, medicine, Physical and Theoretical Chemistry, Kémiai tudományok, Pyrenophorol

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26422625e2674a52dc355f7b474d358a
https://doi.org/10.1002/ejoc.200601128

المؤلفون: Naresh Kumar Vuppula, Sridhar Pervaram, Venkata Ramana Reddy Chittireddy, Dongamanti Ashok, Sreenivasulu Reddymasu

المصدر: Chemical Papers. 72:979-979

مصطلحات موضوعية: Chemistry, General Chemical Engineering, Materials Chemistry, Organic chemistry, Total synthesis, Stereoselectivity, General Chemistry, Biochemistry, Industrial and Manufacturing Engineering, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b5c3ef3f795831bc4e088cae6657aaa9
https://doi.org/10.1007/s11696-017-0351-0

المؤلفون: Subrata Chattopadhyay, Sucheta Chatterjee, Anubha Sharma, Sneha Ghadigaonkar, Payel Sur

المصدر: The Journal of organic chemistry. 79(17)

مصطلحات موضوعية: Molecular Structure, Stereochemistry, Acylation, Organic Chemistry, Diol, Enantioselective synthesis, Stereoisomerism, Tetrahydropyran, Lipase, Ketones, Decarestrictine L, Catalysis, chemistry.chemical_compound, Heterocyclic Compounds, 1-Ring, Lactones, chemistry, Stagonolide E, Heterocyclic Compounds, Organic chemistry, Macrolides, Ene reaction, Pyrenophorol, Pyrans

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9565f55ec3c10a4a904c2c6513f64e07
https://pubmed.ncbi.nlm.nih.gov/25116794

المؤلفون: U.V. Subba Reddy, Jhillu S. Yadav, B. V. Subba Reddy

المصدر: Tetrahedron Letters. 50:5984-5986

مصطلحات موضوعية: Hydrolysis, Chemistry, Stereochemistry, Organic Chemistry, Drug Discovery, Horner–Wadsworth–Emmons reaction, Organic chemistry, Total synthesis, Stereoselectivity, Biochemistry, Pyrenophorol, Kinetic resolution

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6bd94ba3a391f48370567fe0d5b4fb95
https://doi.org/10.1016/j.tetlet.2009.07.047

المؤلفون: Y. Le Floc'h, Sonia J. Amigoni

المصدر: Tetrahedron: Asymmetry. 8:2827-2831

مصطلحات موضوعية: Inorganic Chemistry, chemistry.chemical_classification, Double bond, chemistry, Stereochemistry, Yield (chemistry), Organic Chemistry, Synthon, Total synthesis, Physical and Theoretical Chemistry, Catalysis, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::36f567789caaf06392801da0412d871f
https://doi.org/10.1016/s0957-4166(97)00339-x

المؤلفون: Chihiro Kibayashi, Nobuo Machinaga

المصدر: Tetrahedron Letters. 34:841-844

مصطلحات موضوعية: Enantiopure drug, Chemistry, Stereochemistry, Block (telecommunications), Organic Chemistry, Drug Discovery, Pyrenophorin, Total synthesis, Organic chemistry, Biochemistry, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f0ff44329e7c9fac9d73c47f7f4af970
https://doi.org/10.1016/0040-4039(93)89027-n

المؤلفون: Lambertus Thijs, Binne Zwanenburg, F. J. Dommerholt

المصدر: ChemInform. 23

مصطلحات موضوعية: Chemistry, Stereochemistry, Total synthesis, General Medicine, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fc246a265dda7bae581ad4618ee90349
https://doi.org/10.1002/chin.199202242

المؤلفون: Sonia Amigoni, Y. Le Floc'h

المصدر: ChemInform. 29

مصطلحات موضوعية: Chemistry, Organic chemistry, Total synthesis, General Medicine, Pyrenophorol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::49754383841621f02ceabf8e751b86e1
https://doi.org/10.1002/chin.199806263

المؤلفون: Brian W. Skelton, Allan H. White, Emilio L. Ghisalberti, Jaih R. Hargreaves

المصدر: ChemInform. 33

مصطلحات موضوعية: chemistry.chemical_compound, Chemistry, Stereochemistry, Metabolite, medicine, Identity (social science), General Medicine, Anthelmintic, Byssochlamys nivea, Pyrenophorol, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7a4caa4871ae7ff93dea7e0d3b7fa4d2
https://doi.org/10.1002/chin.200245215

المؤلفون: Xiufeng Zhang, Xiaoyan Pang, Liping Zhang, Yanqin Li, Yongxiang Song, Hua Xiao, Yonghong Liu, Junfeng Wang, Yan Yan

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Marine Biology, Infectious Diseases, Computational Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, unsaturated moiety within, mutagenesis experiments combined, genome mining uncovers, catalyzed isomerization process, distinctive flavoenzyme pyle, genome mining, subsequently elucidated, pyrenophorol dilactones, molecular docking, membered dilactones, including pyrenophorol, dilactone scaffold, derived fungus, catalytic mechanism, biosynthetic pathway, asymmetric 16

Relation: https://figshare.com/articles/journal_contribution/Genome_Mining_Uncovers_a_Flavoenzyme-Catalyzed_Isomerization_Process_during_the_Maturation_of_Pyrenophorol_Dilactones/25250703

الاتاحة: https://doi.org/10.1021/acs.orglett.4c00008.s001
https://figshare.com/articles/journal_contribution/Genome_Mining_Uncovers_a_Flavoenzyme-Catalyzed_Isomerization_Process_during_the_Maturation_of_Pyrenophorol_Dilactones/25250703