about
Higginsianins A and B, Two Diterpenoid α-Pyrones Produced by Colletotrichum higginsianum, with in Vitro Cytostatic Activity.Absolute configurational assignments of secondary amines by CD-sensitive dimeric zinc porphyrin host.Solution versus solid-state structure of ytterbium heterobimetallic catalysts.Determination of absolute configuration of acyclic 1,2-diols with [Mo2(OAc)4], part 2: new structural evidence toward a rationale of the method: what remains of [Mo2(OAc)4] in DMSO solution?Cyclodextrins as carriers for kavalactones in aqueous media: spectroscopic characterization of (S)-7,8-dihydrokavain and beta-cyclodextrin inclusion complex.New mono- and dimeric members of the secalonic acid family: blennolides A-G isolated from the fungus Blennoria sp.Separation of Betti Reaction Product Enantiomers: Absolute Configuration and Inhibition of Botulinum Neurotoxin AInteractions of the organogold(III) compound Aubipyc with the copper chaperone Atox1: a joint mass spectrometry and circular dichroism investigation.Application of electronic circular dichroism in configurational and conformational analysis of organic compounds.Structural and chiroptical properties of the two coordination isomers of YbDOTA-type complexes.Probing molecular chirality by CD-sensitive dimeric metalloporphyrin hosts.Absolute structural elucidation of natural products--a focus on quantum-mechanical calculations of solid-state CD spectra.Conformational aspects in the studies of organic compounds by electronic circular dichroism.Application of electronic circular dichroism in the study of supramolecular systems.Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra.Application of the Ugi reaction with multiple amino acid-derived components: synthesis and conformational evaluation of piperazine-based minimalist peptidomimetics.Isolation, stereochemical study, and cytotoxic activity of isobenzofuran derivatives from a marine Streptomyces sp.Lignans from Schisandra sphenathera Rehd. et Wils. and semisynthetic schisantherin A analogues: absolute configuration, and their estrogenic and anti-proliferative activity.Structure and absolute configuration of new diterpenes from Lavandula multifida.The "Case of Two Compounds with Similar Configuration but Nearly Mirror Image CD Spectra" Refuted. Reassignment of the Absolute Configuration of N-Formyl-3',4'-dihydrospiro[indan-1,2'(1'H)-pyridine].Biological evaluation and determination of the absolute configuration of chloromonilicin, a strong antimicrobial metabolite isolated from Alternaria sonchi.Exciton circular dichroism in channelrhodopsin.Wightianines A-E, dihydro-β-agarofuran sesquiterpenes from Parnassia wightiana, and their antifungal and insecticidal activities.In situ assembly of octahedral Fe(II) complexes for the enantiomeric excess determination of chiral amines using circular dichroism spectroscopy.Chiral/ring closed vs. achiral/open chain triazine-based organogelators: induction and amplification of supramolecular chirality in organic gels.Cis-diastereoselectivity in pictet-spengler reactions of L-tryptophan and electronic circular dichroism studies.[Ln(binolam)3]·(OTf)3, a new class of propeller-shaped lanthanide(III) salt complexes as enantioselective catalysts: structure, dynamics and mechanistic insight.Metabolites from the fungus Phoma sp. 7210, associated with Aizoon canariense.Structure and absolute configuration of toxic polyketide pigments from the fruiting bodies of the fungus Cortinarius rufo-olivaceusSystematic investigation of CD spectra of aryl benzyl sulfoxides interpreted by means of TDDFT calculations.Determination of the absolute configurations at stereogenic centers in the presence of axial chirality.Xanthones and oxepino[2, 3-b]chromones from three endophytic fungi.Determination of absolute configuration of acyclic 1,2-diols with Mo2(OAc)4. 1. Snatzke's method revisited.Strong intermolecular exciton couplings in solid-state circular dichroism of aryl benzyl sulfoxides.Solution and biologically relevant conformations of enantiomeric 11-cis-locked cyclopropyl retinals.Assignment of absolute configuration of chiral carboxylic acids via exciton-coupled CD treatment: 4-phenylthioproline as a case study.Structural and stereochemical studies of alpha-methylene-gamma-lactone-bearing cembrane diterpenoids from a south china sea soft coral Lobophytum crassum.Theoretical analysis of the porphyrin-porphyrin exciton interaction in circular dichroism spectra of dimeric tetraarylporphyrins.Assignment of absolute configuration of a chiral phenyl-substituted dihydrofuroangelicin.Absolute stereochemistry of dihydrofuroangelicins bearing C-8 substituted double bonds: a combined chemical/exciton chirality protocol.
P50
Q28830214-05973B53-6EC6-49B6-8387-25B46CE6D96CQ29393859-A6C53189-875D-494D-B9F4-C7278F73126DQ30789743-CA1C06C4-05ED-4C34-A643-B7D314549152Q30910700-11EBB5FB-A7E3-46FD-9F0C-18A7BB25B7C6Q33534561-4C80AF35-C57A-4DDD-941D-94B6D7428F16Q34772116-FED7ADC9-BDAF-4CEE-84B2-C5955A074173Q35552827-8DCAC61A-F926-4995-BDE1-6F34C78056D2Q35802238-8CEFCF45-722A-43B3-840B-F85E88D0AD34Q36834095-751CC303-FB04-4F3E-897E-3160B9F50108Q37283913-FAF742FF-0FB8-4FB9-A579-62626E25BD34Q37609976-09CDBA2D-E1BC-47D0-BFF7-212C8BCF33A9Q37630432-46E742AC-EF4A-4DAC-B5B1-F970B70D303BQ37890260-BB09822C-2A8E-4533-B0B9-5AD9C54319CBQ38211609-9D4BB372-A1AB-462D-B9D0-75CD42FCCB2CQ38813280-8E796F5A-EAD8-495A-BDD6-8AB55B505F4DQ38893407-E1D31406-22C6-4EF1-B6B6-4C40EE6522DFQ38947865-351E4EF2-1E0C-4C60-9D43-5ABF5BDEAD16Q39226723-7D4E0042-6C13-4D5A-9B5F-C2B0503968CDQ39362255-215D1561-FEF2-4ED6-B0F8-A2DC1336957CQ39554811-ACA43A1F-98D5-4E52-965F-F4E1492751AAQ40737504-CF7D0616-C83B-4E55-98F6-1FBBA976C3B1Q42001495-30D16B30-401D-4E2A-8688-AC74FB3B6593Q42002967-795E9B57-4519-4380-AF62-97AEB37A603BQ42540411-28DFCF8E-8189-49CB-BE1F-0BF769F91D6FQ42654701-F524445D-D05E-467E-BAC8-C6AE995D561AQ42657034-7BFC5694-AC7D-43F2-A67A-A107A187F1C6Q42854686-F123DEB9-1B43-4ADA-AE6B-FB96592C7F3EQ42908053-F08173EE-B0D3-4D55-AB86-008B7594E048Q43039861-D7FEE4D9-AFAD-4417-9F1E-CC69E8BCD3AEQ43184670-0A17450B-C903-4D1C-BEA5-6BCE26A68753Q43245890-A41ECBA7-A8A0-4079-AF2D-DB97713EF868Q43272166-02B4518B-E208-45C0-BFCD-097047B89A30Q43665848-12A08D23-2C04-4430-A0F0-DFCB365BE19BQ43974264-DB1E32B6-1F17-4E16-A209-B0390AD654B0Q44032916-1EF50209-9826-4B46-942C-B412E4F1BF06Q44069061-24C40D01-41AB-42B8-8545-5BE529ADED7EQ44384539-2CA27B8C-4FB5-4224-9C49-A47CF6BE5A7AQ44481792-7DB1AA67-1326-4382-A3BE-8F8AE596EBE4Q44556669-C0557EC2-5E8B-40F7-A607-7B2C7F51F379Q44737905-9959F6E0-3EC7-4C04-90D7-66ED36126691
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Gennaro Pescitelli
@ast
Gennaro Pescitelli
@en
Gennaro Pescitelli
@es
Gennaro Pescitelli
@nl
Gennaro Pescitelli
@sl
type
label
Gennaro Pescitelli
@ast
Gennaro Pescitelli
@en
Gennaro Pescitelli
@es
Gennaro Pescitelli
@nl
Gennaro Pescitelli
@sl
altLabel
Rino Pescitelli
@en
prefLabel
Gennaro Pescitelli
@ast
Gennaro Pescitelli
@en
Gennaro Pescitelli
@es
Gennaro Pescitelli
@nl
Gennaro Pescitelli
@sl
P214
P1053
G-3536-2010
P106
P1153
6603355295
P21
P214
P31
P3829
P396
IT\ICCU\CFIV\269039
P496
0000-0002-0869-5076
P569
1972-01-01T00:00:00Z
P7859
viaf-307342420