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Conversion of aliphatic amides into amines with [I,I-bis(trifluoroacetoxy)iodo]benzene. 1. Scope of the reaction

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inferred← citeshttps://doi.org/10.2139/ssrn.4496949openalex-extracted
inferred← citeshttps://doi.org/10.1002/(sici)1097-0282(199905)49:6<525::aid-bip10>3.0.co;2-3openalex-snapshot
Conformational analysis of potent sweet taste ligands by NMR and computer simulations
inferred← citeshttps://doi.org/10.1002/0471264180.os066.18openalex-snapshot
H ofmann Rearrangement Under Mildly Acidic Conditions Using [I,I‐Bis(Trifluoroacetoxy)]Iodobenzene: Cyclobutylamine Hydrochloride from Cyclobutanecarboxamide
inferred← citeshttps://doi.org/10.1002/9780470125991.ch7openalex-snapshot
Preparation of Amines
inferred← citeshttps://doi.org/10.1002/9780470638859.conrr076openalex-snapshot
Bergmann Degradation
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07980openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos07980.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos07980.pub3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos07980.pub4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos07980.pub5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118341155.ch3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118560907.ch10openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118909911.ch7openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527619948.ch25openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527620784.ch25aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527621262.ch2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.70377openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.19901021212openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.199014681openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.198519169openalex-snapshot
ChemInform Abstract: CONVERSION OF ALIPHATIC AMIDES INTO AMINES WITH (I,I‐BIS(TRIFLUOROACETOXY)IODO)BENZENE. 1. SCOPE OF THE REACTION
inferred← citeshttps://doi.org/10.1002/cjoc.201090071openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201101784openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19960790602openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.5570390609openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlcr.1747openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/nadc.19910390713openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/prac.19893310325openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/prac.19983400215openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/psc.611openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/tcr.201800066openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/3-540-46114-0_2openalex-snapshot
Reactivities, Properties and Structures
inferred← citeshttps://doi.org/10.1007/3-540-46114-0_8openalex-snapshot
Synthetic Applications (Total Synthesis and Natural Product Synthesis)
inferred← citeshttps://doi.org/10.1007/978-1-4899-7270-5_2openalex-snapshot
B
inferred← citeshttps://doi.org/10.1007/bf00531491openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf02049099openalex-snapshot
127I Mössbauer study of some oxygen bonded iodine(I) and iodine(III) complexes
inferred← citeshttps://doi.org/10.1007/bf02974108openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf03036864openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11224-009-9469-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13361-014-0957-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0014-5793(92)80300-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0143-4179(93)90110-vopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00116-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00209-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00247-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/09012-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/09013-0openalex-snapshot
References to Volume 5
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00172-4openalex-snapshot
Degradation Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00623-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00095-8openalex-snapshot
Oxidative Reactions Mediated by Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.1016/b978-012714975-2/50006-5openalex-snapshot
[Bis(acyloxy)iodo]benzenes
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.06.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2009.03.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.07.092openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.10.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.04.021openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chempr.2022.12.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cjche.2025.12.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejps.2021.105883openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fluid.2026.114849openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.09.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jfluchem.2026.110542openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103447openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2003.12.024openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2005.04.077openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2007.03.144openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2012.06.051openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.07.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.03.066openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.12.071openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.08.079openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153422openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154683openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0013-4686(00)00380-7openalex-snapshot
The electrochemically induced Hofmann rearrangement and its comparison with the classic Hofmann rearrangement
inferred← citeshttps://doi.org/10.1016/s0021-9673(98)00993-5openalex-snapshot
Selective fluorescence derivatization and capillary electrophoretic separation of amidated amino acids
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85285-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(01)89603-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(01)91030-0openalex-snapshot
Total, asymmetric synthesis of hexoses and azasugars branched at C(5).
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)01021-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(98)00416-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00071-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)76945-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85230-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)88474-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)93601-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)97227-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00985-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(97)10324-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0065-2725(03)86004-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0960-894x(00)80424-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.0c02767openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.7b00122openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00675openalex-snapshot
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Rearrangement of α-Amino Cyclopropanone Hydrate: A Novel Route to Labeled Amino Acids
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A Dimethyl Ketal-Protected Benzoin-Based Linker Suitable for Photolytic Release of Unprotected Peptides
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Iodine(III)-Promoted Ring Contraction of 1,2-Dihydronaphthalenes: A Diastereoselective Total Synthesis of (±)-Indatraline
inferred← citeshttps://doi.org/10.1021/ol101993qopenalex-snapshot
Hofmann Rearrangement of Carboxamides Mediated by Hypervalent Iodine Species Generated in Situ from Iodobenzene and Oxone: Reaction Scope and Limitations
inferred← citeshttps://doi.org/10.1021/ol991264xopenalex-snapshot
The Total Synthesis of Pantocin B
inferred← citeshttps://doi.org/10.1021/op2000207openalex-snapshot
An Efficient Process for the Manufacture of Carmegliptin
inferred← citeshttps://doi.org/10.1038/s41557-025-01848-2openalex-snapshot
Accessing sulfonamides via formal SO2 insertion into C–N bonds
inferred← citeshttps://doi.org/10.1038/s41557-025-01904-xopenalex-snapshot
Carbon-to-nitrogen atom swap enables direct access to benzimidazoles from drug-like indoles
inferred← citeshttps://doi.org/10.1039/a808466aopenalex-snapshot
Novel metal complex synthons for chiral 4-azaleucine, 2,3-diaminopropanoic acid and its elaboration
inferred← citeshttps://doi.org/10.1039/a904126eopenalex-snapshot
New reaction conditions using trifluoroethanol for the E-I Hofmann rearrangement
inferred← citeshttps://doi.org/10.1039/a909898dopenalex-snapshot
Synthetic studies on the pederin family of antitumour agents. Syntheses of mycalamide B, theopederin D and pederin
inferred← citeshttps://doi.org/10.1039/b415543bopenalex-snapshot
Design and synthesis of a new class of arginine analogues with an improved anion binding site in the side chain
inferred← citeshttps://doi.org/10.1039/b801909fopenalex-snapshot
Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement
inferred← citeshttps://doi.org/10.1039/b914580jopenalex-snapshot
The coumarin→indole transformation—a method for preparing 4-halo-5-hydroxyindoles from coumarins
inferred← citeshttps://doi.org/10.1039/b922033jopenalex-snapshot
Hypervalent N-sulfonylimino-λ3-bromane: active nitrenoid species at ambient temperature under metal-free conditions
inferred← citeshttps://doi.org/10.1039/c1np00028dopenalex-snapshot
Hypervalent iodine reagents in the total synthesis of natural products
inferred← citeshttps://doi.org/10.1039/c2cc16360hopenalex-snapshot
A catalytic version of hypervalent aryl-λ 3 -iodane-induced Hofmann rearrangement of primary carboxamides: iodobenzene as an organocatalyst and m-chloroperbenzoic acid as a terminal oxidant
inferred← citeshttps://doi.org/10.1039/c3cy00934copenalex-snapshot
Rearrangement of aldoximes to amides in water under air atmosphere catalyzed by water-soluble iridium complex [Cp*Ir(H 2 O) 3 ][OTf] 2
inferred← citeshttps://doi.org/10.1039/c4nj01668hopenalex-snapshot
Synthesis of unsymmetrical phenylurea derivatives via oxidative cross coupling of aryl formamides with amines under metal-free conditions
inferred← citeshttps://doi.org/10.1039/c7cc05160copenalex-snapshot
Iodoarene-catalyzed oxidative transformations using molecular oxygen
inferred← citeshttps://doi.org/10.1039/cc9960001933openalex-snapshot
Synthesis and nucleophilic substitution of allenyl(m-nitrophenyl)iodanes as a new propynyl cation-equivalent species: synthesis of propynyl ethers, esters, and amides
inferred← citeshttps://doi.org/10.1039/d0cc05354fopenalex-snapshot
Hypervalent iodine reagent-mediated reactions involving rearrangement processes
inferred← citeshttps://doi.org/10.1039/d0ce00368aopenalex-snapshot
A crystalline solid adduct of sulfathiazole–amantadine: the first dual-drug molecular salt containing both antiviral and antibacterial ingredients
inferred← citeshttps://doi.org/10.1039/d1ce00382hopenalex-snapshot
Molecular adduct of amantadine ferulate presents a pathway for slowing in vitro / vivo releases and raising synergistic antiviral effects via dual optimization salification strategy
inferred← citeshttps://doi.org/10.1039/d1nj03160kopenalex-snapshot
Synthesis of unsymmetrical urea from aryl- or pyridyl carboxamides and aminopyridines using PhI(OAc) 2 via in situ formation of aryl- or pyridyl isocyanates
inferred← citeshttps://doi.org/10.1039/d3ob01964kopenalex-snapshot
Phenyliodine bis(trifluoroacetate) as a sustainable reagent: exploring its significance in organic synthesis
inferred← citeshttps://doi.org/10.1039/d5qo00173kopenalex-snapshot
Iron-catalyzed regioselective carboazidation of alkenes for the synthesis of multi-substituted cyclobutylamines
inferred← citeshttps://doi.org/10.1039/p19920002633openalex-snapshot
Synthesis of two 6′α-fluorocarbocyclic nucleosides and incorporation into short segments of DNA
inferred← citeshttps://doi.org/10.1055/s-0040-1707103openalex-snapshot
A Straightforward Synthesis of N-Substituted Ureas from Primary Amides
inferred← citeshttps://doi.org/10.1080/00397910701877608openalex-snapshot
Fast and Efficient Access to a Family of Multifunctional 1,3,5-Trisubstituted Piperidines
inferred← citeshttps://doi.org/10.1080/00397910802398256openalex-snapshot
Novel Route toN-Acyl-N′-formyl Aminal
inferred← citeshttps://doi.org/10.1080/00397910903097229openalex-snapshot
Convenient, Solvent-Free Method for Preparation of [Hydroxy(phosphoryloxy)iodo]arenes
inferred← citeshttps://doi.org/10.1080/00397918808081322openalex-snapshot
Synthesis of Aliphatic Amines Related to Monodansylcadaverine Via the Oxidative Rearrangement of Aliphatic Amides with Phenyl Iodosyl Bis(Trifluoroacetate)
inferred← citeshttps://doi.org/10.1080/07328319008045192openalex-snapshot
5′-C-Chain-Extended Adenosine Derivatives Related to Sinefungin. Synthesis and Biological Activity
inferred← citeshttps://doi.org/10.1080/07328319608007381openalex-snapshot
Relationship Between Chemical Structure and Antileishmanial Effect of Sinefungine Analogues
inferred← citeshttps://doi.org/10.1081/scc-120021988openalex-snapshot
Conversion of a Ketone to a Geminal Bisacetamide: Synthesis of 1,1-Bisacetamidocyclohexane
inferred← citeshttps://doi.org/10.1111/j.1399-3011.1990.tb01300.xopenalex-snapshot
Cyclic hexapeptides related to somatostatin Synthesis and biological testing
inferred← citeshttps://doi.org/10.1111/j.1399-3011.2005.00224.xopenalex-snapshot
Exploring the stereochemical requirements for protease inhibition by ureidopeptides
inferred← citeshttps://doi.org/10.1246/bcsj.79.142openalex-snapshot
Direct and Convenient Synthesis of [Bis(trifluoroacetoxy)iodo]arenes from Iodoarenes
inferred← citeshttps://doi.org/10.24820/ark.5550190.p010.975openalex-snapshot
Iodonium imides in organic synthesis
inferred← citeshttps://doi.org/10.3390/molecules16119421openalex-snapshot
Indatraline: Synthesis and Effect on the Motor Activity of Wistar Rats
inferred← citeshttps://doi.org/10.3987/com-18-s(f)43openalex-snapshot
[Bis(trifluoroacetoxy)iodo]p-nitrobenzene and [Bis(trifluoroacetoxy)iodo]pentafluorobenzene as Lead Reagents for the Direct Ring Contraction of Lactams to Pyrrolidines
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