About: Josep Bonjoch

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh)
rdfs:label	Josep Bonjoch (en) Josep Bonjoch (es) Josep Bonjoch (nl) Josep Bonjoch (ast)
skos:prefLabel	Josep Bonjoch (en) Josep Bonjoch (es) Josep Bonjoch (nl) Josep Bonjoch (ast)
name	Josep Bonjoch (en) Josep Bonjoch (es) Josep Bonjoch (nl) Josep Bonjoch (ast)
Scopus author ID	wds:Q59550420-A08F8E90-AF04-4D8A-805A-65813DDEB68C
Scopus author ID	7005721785
given name	wds:Q59550420-6004DE5C-E395-40FF-B2CE-2B7E4E2ADFDB
given name	Josep
instance of	wds:Q59550420-329B437B-5392-4F64-ADC5-BA69E49F18D6
instance of	Homo sapiens
occupation	wds:Q59550420-76F910FB-F051-41A5-819A-BF8B79E2171D
University of Barcelona authority ID	wds:Q59550420-8EF9F19B-8286-4B6C-8B0E-7FE23AE11555
University of Barc...D (former scheme)	wds:Q59550420-339AC8B6-FB3A-4E8C-99D5-5E8E7340843E
sex or gender	wds:Q59550420-BDE9D788-E7AE-46C8-8D04-E95B4D2C0E95
VIAF ID	wds:Q59550420-101FFD67-CD25-4540-88EC-86FE4D5DB361
CANTIC ID	wds:Q59550420-46B7D153-2203-4067-8DD9-2A60FA811E17
VIAF ID	http://viaf.org/viaf/305873187
occupation	researcher
University of Barcelona authority ID	981058510132906706
University of Barc...D (former scheme)	a1022282
sex or gender	male
VIAF ID	305873187
CANTIC ID	981058510132906706
ORCID iD	wds:Q59550420-A7AA40A9-1092-4738-BEC9-9EED728CC892
ORCID iD	https://orcid.org/0000-0002-5551-6720
ORCID iD	0000-0002-5551-6720
ResearcherID	wds:Q59550420-961BCA89-5061-4E62-90E2-0D51FC1AC09F
ResearcherID	C-1429-2014
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59550420
is author of	Biosynthesis and structure of aeruginoside 126A and 126B, cyanobacterial peptide glycosides bearing a 2-carboxy-6-hydroxyoctahydroindole moiety Total synthesis of aignopsanes, a class of sesquiterpenes: (+)-aignopsanoic acid A, (-)-methyl aignopsanoate A, and (-)-isoaignopsanoic A. Polycyclic framework synthesis of anominine and tubingensin A indole diterpenoids. Synthesis and biological evaluation of a conformationally free seco-analogue of the immunosuppressant FR901483 Asymmetric synthesis of 2-azabicyclo[3.3.1]nonanes by a microwave-assisted organocatalysed tandem desymmetrisation and intramolecular aldolisation. Synthesis of Strychnine. Total Synthesis of (-)-Strychnine via the Wieland-Gumlich Aldehyde Slow interconversion of enantiomeric conformers or atropisomers of anilide and urea derivatives of 2-substituted anilines. Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones. Intramolecular Pd-mediated processes of amino-tethered aryl halides and ketones: insight into the ketone alpha-arylation and carbonyl-addition dichotomy. A new class of four-membered azapalladacycles Atom transfer radical cyclization of trichloroacetamides to electron-rich acceptors using Grubbs' catalysts: synthesis of the tricyclic framework of FR901483 Synthesis of the 4-azatricyclo[5.2.2.0(4,8)]undecan-10-one core of daphniphyllum alkaloid calyciphylline A using a Pd-catalyzed enolate alkenylation Nitrogen heterocycles by palladium-catalyzed cyclization of amino-tethered vinyl halides and ketone enolates Total synthesis of (-)-anominine Synthesis and structure-activity relationships of gamma-carboline derivatives as potent and selective cysLT(1) antagonists. Synthetic and DFT studies towards a unified approach to phlegmarine alkaloids: aza-Michael intramolecular processes leading to 5-oxodecahydroquinolines Ring Expansion of Functionalized Octahydroindoles to Enantiopurecis-Decahydroquinolines† A gram-scale route to phlegmarine alkaloids: rapid total synthesis of (-)-cermizine B. Synthesis and evaluation of novel boron-containing complexes of potential use for the selective treatment of malignant melanoma Syntheses of both the putative and revised structures of aeruginosin EI461 bearing a new bicyclic alpha-amino acid Decahydroquinoline Ring 13C NMR Spectroscopic Patterns for the Stereochemical Elucidation of Phlegmarine-Type Lycopodium Alkaloids: Synthesis of (-)-Serralongamine A and Structural Reassignment and Synthesis of (-)-Huperzine K and (-)-Huperzine M (L Organocatalyzed asymmetric synthesis of morphans Total Synthesis of (+/-)-Deethylibophyllidine: Studies of a Fischer Indolization Route and a Successful Approach via a Pummerer Rearrangement/Thionium Ion-Mediated Indole Cyclization Synthesis of the tetracyclic ABCD ring systems of madangamines D-F. Cu(I)-catalyzed atom transfer radical cyclization of trichloroacetamides tethered to electron-deficient, -neutral, and -rich alkenes: synthesis of polyfunctionalized 2-azabicyclo[3.3.1]nonanes Stereocontrolled Synthesis of the Daphenylline Pentacyclic ACDEF Ring System Iron-Catalyzed Radical Intermolecular Addition of Unbiased Alkenes to Aldehydes Radical Cyclization of Alkene-Tethered Ketones Initiated by Hydrogen-Atom Transfer. Intramolecular radical non-reductive alkylation of ketones via transient enamines. Synthesis of the Tetracyclic ABCD Ring Domain of Calyciphylline A-Type Alkaloids via Reductive Radical Cyclizations. NMR evidence of the kinetic and thermodynamic products in the NIS promoted cyclization of 1-phenyl-4-pentenylamines. Synthesis and reactivity of trans-2-phenyl-5-iodopiperidines Decarbonylative radical cyclization of alpha-amino selenoesters upon electrophilic alkenes. A general method for the 6-azabicyclo[3.2.1]octane synthesis. Total Synthesis of the Strychnos Alkaloids (+/-)-Akuammicine and (+/-)-Norfluorocurarine from 3a-(o-Nitrophenyl)hexahydroindol-4-ones by Nickel(0)-Promoted Double Cyclization Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine E and Putative Structure of (-)-Huperzine N. Synthesis of (±)-Serralongamine A and the Revised Structure of Huperzine N. Synthesis of -hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation cis-Decahydroquinolines via asymmetric organocatalysis: application to the total synthesis of lycoposerramine Z Iron Hydride Radical Reductive Alkylation of Unactivated Alkenes New insights into NIS-promoted aminocyclization. Synthesis of decahydroquinolines from 2-allylcyclohexylamines Translocation versus cyclisation in radicals derived from N-3-alkenyl trichloroacetamides Synthesis of α-Chlorolactams by Cyanoborohydride-Mediated Radical Cyclization of Trichloroacetamides
is author of	wds:Q30864033-8D92F926-808C-4183-AD36-ADA2FACF5E41 wds:Q52929319-5031A59A-632C-4E02-8CD0-11A27065AD5E wds:Q78889200-265BE819-33CA-4EE1-A49E-D98BCD7D919D wds:Q85278876-6A14F3F8-EDA9-471D-B21F-C9D79E621D78 wds:Q92637643-7BD2207A-D437-4BCD-8DB1-008B07EB110A wds:Q85849252-3BA3D835-A198-4352-833E-8A2F8BAEE8D9 wds:Q86686416-FC06F450-73EA-4214-8D93-60D28F8051A7 wds:Q39934195-1087B064-D54E-4D5F-8AC0-223CE1B5FA85 wds:Q51375240-03FC1683-67D0-4B79-99E5-2C3631FCD8A6 wds:Q81481967-D04EE9B2-1B8C-46BB-ABEA-1AF5A0AB6341 wds:Q91545476-3C444785-0ED0-49D4-BFC1-F5CED6B75B99 wds:Q100446491-793A6CAF-0A7B-4258-A9B9-2DEA2BEE99D5 wds:Q46761610-3F41407A-C351-4F0B-8B7A-5AB78C9A67A2

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