المؤلفون: Pengzhi Wang (149230), Jonathan S. Lindsey (1581841)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Evolutionary Biology, Infectious Diseases, Chemical Sciences not elsewhere classified, 3- position, Bacteriochlorophylls Native chlorop., bacterio, carboxylic acid group, tert, Schreiber-modified Nicholas reaction, native-like D-ring substituents, Jacobi Pd-mediated lactone formation, CO, butyldiphenylsilyl-protected propan., tailorable A-ring substituents, dialkyl-substituted pent -4-ynoic acid

Relation: https://figshare.com/articles/journal_contribution/Synthesis_of_AD-Dihydrodipyrrins_Equipped_with_Latent_Substituents_of_Native_Chlorophylls_and_Bacteriochlorophylls/15109069

الاتاحة: https://doi.org/10.1021/acs.joc.1c01239.s001

المؤلفون: Ivan M. Novitskiy (2122903), Andrei G. Kutateladze (1344246)

مصطلحات موضوعية: Biophysics, Biochemistry, Physiology, Pharmacology, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, nmr spectra revealed, natural products containing, containing natural products, computationally driven revisions, relatively common error, proposed anhydride moiety, misassigned structures featured, common challenge, carboxylic anhydride, structure assignment, lactone formation, hydroxy group

Relation: https://figshare.com/articles/journal_contribution/DU8_Computations_Reveal_a_Common_Challenge_in_the_Structure_Assignment_of_Natural_Products_Containing_a_Carboxylic_Anhydride_Moiety/16948544

الاتاحة: https://doi.org/10.1021/acs.joc.1c02291.s001

المؤلفون: Andrei G. Kutateladze, Ivan M. Novitskiy

المصدر: The Journal of organic chemistry. 86(23)

مصطلحات موضوعية: Biological Products, Magnetic Resonance Spectroscopy, Common error, Molecular Structure, Lactone formation, Stereochemistry, Organic Chemistry, Hydroxy group, Structure (category theory), Anhydrides, NMR spectra database, chemistry.chemical_compound, chemistry, Moiety

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c627941f9f50dbf50e90fc2a7c0b66ba
https://pubmed.ncbi.nlm.nih.gov/34743508

المؤلفون: Kazuaki Matsumoto, Xiaoxi Liu, Yoo Tanabe, Mizuki Moriyama, Yuki Enoki

المصدر: Pharmaceuticals, Vol 14, Iss 938, p 938 (2021)
Pharmaceuticals
Volume 14
Issue 9

مصطلحات موضوعية: anti-MRSA activity, plymuthipyranone B, Mukaiyama aldol addition, chiral discrimination, Chemistry, Stereochemistry, Lactone formation, Pharmaceutical Science, enantiomers, Anti mrsa, Catalysis, Synthetic analogue, RS1-441, Pharmacy and materia medica, Yield (chemistry), Drug Discovery, asymmetric total syntheses, Molecular Medicine, Medicine, Enantiomer, Enantiomeric excess

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb6d0fc871468cb1996d293acee91ab
https://www.mdpi.com/1424-8247/14/9/938

المؤلفون: Zhi Guan, Jia-Yi Gu, Wei Zhang, Yan-Hong He, Seth R. Jackson

المصدر: Chemical Communications. 56:13441-13444

مصطلحات موضوعية: Proton, Lactone formation, Aromatic ketones, Intermolecular force, Metals and Alloys, General Chemistry, Transesterification, Medicinal chemistry, Catalysis, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, Umpolung, chemistry.chemical_compound, Ketyl, chemistry, Intramolecular force, Materials Chemistry, Ceramics and Composites

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee518177af87eb5144d2aa3cf1b84d5a
https://doi.org/10.1039/d0cc05306f

المؤلفون: Valentin S. Enev, Peter Gärtner, Maximilian Kaiser

المصدر: Monatshefte für Chemie - Chemical Monthly. 148:49-56

مصطلحات موضوعية: Chiral auxiliary, 010405 organic chemistry, Chemistry, Stereochemistry, Lactone formation, Enantioselective synthesis, General Chemistry, 010402 general chemistry, 01 natural sciences, 0104 chemical sciences, chemistry.chemical_compound, Amide, Michael reaction, Orthoester

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::aebd08c2b52fa1b112bbbf161877ae95
https://doi.org/10.1007/s00706-016-1858-8

المؤلفون: Nanami Sugiyama, Takuya Maeda, Satoshi Yokojima, Yasuo Dobashi, Daisuke Yuyama, Hikaru Yanai, Takashi Matsumoto, Yuuki Fujimoto

المصدر: Synlett. 27:1949-1956

مصطلحات موضوعية: chemistry.chemical_classification, 010405 organic chemistry, Lactone formation, Stereochemistry, organic chemicals, Organic Chemistry, 010402 general chemistry, 01 natural sciences, 0104 chemical sciences, Stereocenter, chemistry, Side chain, heterocyclic compounds, Alkanoic acid, hormones, hormone substitutes, and hormone antagonists, Lactone

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07363c430a335a5cac26b440d0f63756
https://doi.org/10.1055/s-0035-1561477

المؤلفون: Naohiro Gotoh, Arisa Tago, Toshiharu Nagai, Yasunari Kato, Kazuaki Yoshinaga, Junji Obi, Akihiko Yoshida

المصدر: Food chemistry. 274

مصطلحات موضوعية: Spectrometry, Mass, Electrospray Ionization, Silylation, 01 natural sciences, Analytical Chemistry, Lactones, 0404 agricultural biotechnology, Isomerism, Tandem Mass Spectrometry, Hydroxy fatty acid, Animals, Triglycerides, chemistry.chemical_classification, Chromatography, Chemistry, Lactone formation, 010401 analytical chemistry, Fatty Acids, 04 agricultural and veterinary sciences, General Medicine, 040401 food science, 0104 chemical sciences, Liquid chromatography electrospray ionization tandem mass spectrometry, Milk, Milk fat, lipids (amino acids, peptides, and proteins), Lactone, Food Science, Chromatography, Liquid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b35ecdc6d8ad1662d8b78f7f473e7218
https://pubmed.ncbi.nlm.nih.gov/30372942

المؤلفون: Yasuyuki Kita, Naohiko Washimi, Tohru Kamitanaka, Hitoho Takamuro, Yusuke Mishima, Toshifumi Dohi

المصدر: Tetrahedron Letters. 56:3046-3051

مصطلحات موضوعية: Silylation, Lactone formation, Organic Chemistry, Acetal, Aromatization, Silyl enol ether, Biochemistry, Enol, Quinone, Solvent, chemistry.chemical_compound, chemistry, Drug Discovery, Organic chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3ada68bba09af97f17311c5f3d943036
https://doi.org/10.1016/j.tetlet.2014.11.085

المؤلفون: Hidetaka Tsujimoto, Suguru Higashida, Teruyuki Miyake, Michio Matsumura, Ryusei Oketani, Takuya Fukui, Seihou Jinnai

المصدر: Chemistry Letters. 45:801-803

مصطلحات موضوعية: Decarboxylation, Lactone formation, High selectivity, 02 engineering and technology, General Chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Photocatalysis, Organic chemistry, Molecular oxygen, 0210 nano-technology, Acetonitrile, Diphenic acid, Benzoic acid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::1bb4fa04cd1271275901b5f56bba8442
https://doi.org/10.1246/cl.160237

المؤلفون: Dieter Schinzer, Lars Michaelis

المصدر: Synlett. 25:951-954

مصطلحات موضوعية: Core (optical fiber), chemistry.chemical_compound, Lactone formation, Chemistry, Stereochemistry, Organic Chemistry, Enantioselective synthesis, Total synthesis, Epoxide, Octane

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::539d29e21b3251a7adc61d89da9f5a9f
https://doi.org/10.1055/s-0033-1340182

المؤلفون: Nopporn Thasana, Somsak Ruchirawat, Prattya Nealmongkol, Kassrin Tangdenpaisal, Somkid Sitthimonchai

المصدر: Tetrahedron. 69:9277-9283

مصطلحات موضوعية: Antioxidant, Chemistry, Lactone formation, Yield (chemistry), medicine.medical_treatment, Organic Chemistry, Drug Discovery, medicine, Organic chemistry, chemistry.chemical_element, Bond formation, Biochemistry, Copper

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::78b99744a32b91ebabcd2777f263e4a0
https://doi.org/10.1016/j.tet.2013.08.045

المؤلفون: Gowravaram Sabitha, K. Shankaraiah, Jhillu S. Yadav

المصدر: European Journal of Organic Chemistry. 2013:4870-4878

مصطلحات موضوعية: chemistry.chemical_compound, Natural product, Synargentolide B, chemistry, Tandem, Lactone formation, Stereochemistry, Organic Chemistry, Diastereomer, Stereoselectivity, Physical and Theoretical Chemistry, Metathesis, Ring (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d295a637bef67f481dc6dee491f53c35
https://doi.org/10.1002/ejoc.201300434

المؤلفون: Paul Ha-Yeon Cheong, Daniel M. Walden, Emily R. T. Robinson, Charlene Fallan, Mark D. Greenhalgh, Andrew D. Smith

المساهمون: The Royal Society, European Commission, University of St Andrews. School of Chemistry, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. EaSTCHEM

المصدر: Chemical Science

مصطلحات موضوعية: chemistry.chemical_classification, 010405 organic chemistry, Lactone formation, Stereochemistry, NDAS, General Chemistry, Benzoxazole, 010402 general chemistry, QD Chemistry, 01 natural sciences, 0104 chemical sciences, Catalysis, Chemistry, chemistry.chemical_compound, chemistry, Nucleophile, Benzothiazole, Lactam, lipids (amino acids, peptides, and proteins), QD, Chemoselectivity, Lactone

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f60553c65a18acda5776739ab78e324d
https://hdl.handle.net/10023/9248

المؤلفون: Jun Kino, Yoshitaka Matsushima

المصدر: Synthesis. 2011:1290-1294

مصطلحات موضوعية: chemistry.chemical_classification, Stereochemistry, Lactone formation, Organic Chemistry, Epoxide, chemistry.chemical_element, Catalysis, chemistry.chemical_compound, chemistry, medicine, Deoxy sugar, Novobiocin, medicine.drug, Palladium

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::850d05ce18214ca43e8fe530352b9b34
https://doi.org/10.1055/s-0030-1258475

المؤلفون: J.P. Ward

المصدر: Recueil des Travaux Chimiques des Pays-Bas. 92:814-818

مصطلحات موضوعية: chemistry.chemical_compound, Bicyclic molecule, Chemistry, Lactone formation, Yield (chemistry), chemistry.chemical_element, Cyclopentene, Organic chemistry, General Chemistry, Zinc, Reformatsky reaction, Benzene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5277d15b5ee4e9b747d75f99f12ed375
https://doi.org/10.1002/recl.19730920802

المؤلفون: Shuhei Takahashi, Tatsuo Okauchi, Mitsuru Kitamura

المصدر: ChemInform. 47

مصطلحات موضوعية: chemistry.chemical_compound, Formal synthesis, Pradimicinone, chemistry, Lactone formation, Insertion reaction, Intramolecular force, Total synthesis, General Medicine, Medicinal chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0d414319640fd7edc8092ca5915ee584
https://doi.org/10.1002/chin.201603137

المؤلفون: Yasuyuki Kita, Akinobu Maruyama, Akihiro Goto, Toshifumi Dohi, Naoko Takenaga

المصدر: Organic Letters. 9:3129-3132

مصطلحات موضوعية: Bromides, Molecular Structure, Potassium Compounds, Lactone formation, Aryl, Organic Chemistry, Carboxylic Acids, Hypervalent molecule, chemistry.chemical_element, Phthalimides, General Medicine, Iodine, Benzoates, Combinatorial chemistry, Biochemistry, Lactones, chemistry.chemical_compound, chemistry, Reagent, Organic chemistry, Indicators and Reagents, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82f46915a08c33e159aed59740d632bc
https://doi.org/10.1021/ol071315n

المؤلفون: Carolyn M. Cammarano, Austin G. Smith, Kevin J. Quinn

المصدر: Tetrahedron. 63:4881-4886

مصطلحات موضوعية: Tandem, Stereochemistry, Chemistry, Lactone formation, Longest linear sequence, Organic Chemistry, Squamostolide, Total synthesis, General Medicine, Highly selective, Metathesis, Combinatorial chemistry, Biochemistry, chemistry.chemical_compound, Drug Discovery, Acetogenin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3409f6bb84ec54480939d223c30cf8c8
https://doi.org/10.1016/j.tet.2007.03.151

المؤلفون: Tatsuo Okauchi, Mitsuru Kitamura, Shuhei Takahashi

المصدر: The Journal of organic chemistry. 80(16)

مصطلحات موضوعية: chemistry.chemical_compound, Formal synthesis, Pradimicinone, Chemistry, Insertion reaction, Lactone formation, Intramolecular force, Organic Chemistry, Organic chemistry, Total synthesis, Combinatorial chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa7f5f26057b9d67e3d2924a87218a6
https://pubmed.ncbi.nlm.nih.gov/26186040