sameAs
Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromaticsStereoselective synthesis of the C1-C11 and C12-C34 fragments of mycalolide AEfficient synthesis of substituted 3-azabicyclo[3.1.0]hexan-2-ones from 2-iodocyclopropanecarboxamides using a copper-free Sonogashira coupling.Total synthesis of (-)-spongidepsin.Monoalkylation of acetonitrile by primary alcohols catalyzed by iridium complexes.Harnessing C-H Activation of Benzhydroxamates as a Macrocyclization Strategy: Synthesis of Structurally Diverse Macrocyclic Isoquinolones.Selective methodologies for the synthesis of biologically active piperidinic compounds.Metathesis reactions. General considerations.H12461. Fluorine as a Regiocontrol Element in the Ring Openings of Bicyclic AziridiniumsTotal Synthesis of Putative 11-epi-Lyngbouilloside Aglycon.Rearrangement of beta-amino alcohols via aziridiniums: a review.Peptides targeting estrogen receptor alpha-potential applications for breast cancer treatment.When cyclopropenes meet gold catalysts.Isolation, structural determination and synthetic approaches toward amphidinol 3.Linchpin dienes: key building-blocks in the synthesis of polyenic frameworks.Iron-Catalyzed C-C Cross-Couplings Using Organometallics.Strength by joining methods: combining synthesis with NMR, IR, and vibrational circular dichroism spectroscopy for the determination of the relative configuration in hemicalide.Mechanism of action of the cytotoxic macrolides amphidinolide X and J.Biological evaluation of newly synthesized quinoline-5,8-quinones as Cdc25B inhibitors.Synthetic Studies toward the C32-C46 Segment of Hemicalide. Assignment of the Relative Configuration of the C36-C42 Subunit.An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A.A versatile route to the tulearin class of macrolactones: synthesis of a stereoisomer of tulearin A.Enantioselective synthesis of β-fluoroamines from β-amino alcohols: application to the synthesis of LY503430.Synthesis of 3-oxa- and 3-azabicyclo[4.1.0]heptanes by gold-catalyzed cycloisomerization of cyclopropenes.Synthetic efforts toward the spiroketal core of spirangien A.Ring-rearrangement metathesis of cyclopropenes: synthesis of heterocycles.QSPR prediction of the stability constants of gadolinium(III) complexes for magnetic resonance imaging.A short synthesis of argatroban. a potent selective thrombin inhibitor.Enantioselective allyltitanations and metathesis reactions. Application to the synthesis of piperidine alkaloids (+)-sedamine and (-)-prosophylline.Free-radical hydroxylation reactions of alkylboronates.Stereoselective synthesis of polypropionate units and heterocyclic compounds by cyclopropylcarbinol ring-opening with mercury(II) salts.Synthesis of the c14-c25 subunit of bafilomycin A1.Total synthesis of zincophorin and its methyl ester.FeCl3·6H2O, a catalyst for the diastereoselective synthesis of cis-isoxazolidines from N-protected δ-hydroxylamino allylic acetates.Rearrangement of beta-amino alcohols and application to the synthesis of biologically active compounds.Highly enantioselective synthesis of linear beta-amino alcohols.Rhodium-Catalyzed Cyclization of O,ω-Unsaturated Alkoxyamines: Formation of Oxygen-Containing Heterocycles.Intramolecular cyclopropanation and C-H insertion reactions with metal carbenoids generated from cyclopropenes.Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of beta-amino alcohols.Stereoselective Ring-Opening of gem-Difluorocyclopropanes: An Entry to Stereo-defined (E,E)- and (E,Z)-Conjugated Fluorodienes.
P50
Q26776183-4C183B5E-EA96-4770-961C-0678FAE95C5EQ28289230-89E8E158-E207-49D7-A591-2472813ECEF9Q34488194-C20D04F4-C4A6-4D03-A8B4-C3CB012D8A64Q34551207-B13B4466-F689-4FD2-ACC3-653DBE7D87EBQ34630836-EA53B32F-1A58-40E4-BBC1-7B02BA174A42Q36028073-D682CEB0-0182-4F50-9857-7651E8BF8F99Q36095997-47340092-B79F-4443-BBCA-D4FFA4125854Q36353804-A03CA8B8-7A77-41BB-83A8-031FC1A30C07Q36652136-BFBFE13B-1863-445C-B8DA-AB397BEA93FAQ37159264-869BEBDF-AC95-47BA-92DD-5FD2A476117AQ37659936-1A3C64C4-C469-4245-868D-27637C2E119EQ37897608-14D10C7D-9025-4311-B0B6-C880D59E65A5Q37909035-18E57EA7-33D6-439C-BF07-25A6B3124D1BQ38188454-920BE51F-DA19-4E5B-84E3-8F629B05C9C7Q38372819-5830DB60-A544-47BD-8B78-C6FA7D97B72DQ38940361-2862C468-0369-40FA-B768-39AEE1B2DE48Q38945014-5B117E7D-80FD-4097-ABC5-A3B18536D858Q39557163-CD0C5804-6C6D-4B88-9847-0769BE039912Q40314867-36ADAC2C-5C49-4BDD-B6F9-310EFD03387DQ41022871-535568DD-2D92-48BA-A36D-DC21C9A8F0B2Q42168127-C6C87E6C-E4F1-42DB-A5C0-B02F44DA1C86Q42254041-29238770-6A58-4FC1-A764-73C53DE83E80Q42904858-69EAEB51-DE65-4226-9CC1-795977FA97ADQ42931260-5331C30F-116B-4C4F-B34A-D84ABF2B832FQ42976268-D3C43C8C-FCD8-4FB6-9B9D-0C31B1E47C5EQ43227554-496BB148-27B4-4D19-9EFC-FA027FBEE0F5Q43418263-9EC14C4F-70C3-4467-8530-0F4BBDABB032Q43675014-DC9ADC9F-DC41-4DED-9345-B608B7A05FBBQ43941419-96EB9E67-6912-4238-8F98-7ADBE780AAB8Q44176426-036CEF9B-CDD5-48A1-9299-9F1C4A63A250Q44624227-5978E49A-13E1-4596-85C8-0C6450454955Q44698132-094B5248-F95E-4745-BB7A-57872FEB1202Q44961143-DBC5D166-8297-4714-8274-60B2C258E558Q45051735-F7CAB074-D8D6-456B-B70B-1DA9B8EF039AQ46029166-FCDCF35F-2852-4FE4-982F-D07C32CC285FQ46196376-BD3C6028-154D-4445-8B49-F72CE6441C02Q46245356-C79BBE85-4909-49FD-B363-812B533ED22EQ46760906-E5B7F3FC-A9D7-4978-96B6-A31F8C78BE85Q46841817-AED1B911-F80E-43E8-B7AD-17C87BC7D358Q48136175-15A5D45C-18EF-4469-BDEF-F0E0CA86708E
P50
description
Frans scheikundige
@nl
French chemist
@en
French chemist
@en-ca
French chemist
@en-gb
Prantsusmaa keemik
@et
ceimiceoir Francach
@ga
chimiste française
@fr
chimistă franceză
@ro
kimiste franceze
@sq
química francesa
@ast
name
Janine Cossy
@ast
Janine Cossy
@ca
Janine Cossy
@da
Janine Cossy
@en
Janine Cossy
@es
Janine Cossy
@fr
Janine Cossy
@hu
Janine Cossy
@nb
Janine Cossy
@nl
Janine Cossy
@nn
type
label
Janine Cossy
@ast
Janine Cossy
@ca
Janine Cossy
@da
Janine Cossy
@en
Janine Cossy
@es
Janine Cossy
@fr
Janine Cossy
@hu
Janine Cossy
@nb
Janine Cossy
@nl
Janine Cossy
@nn
prefLabel
Janine Cossy
@ast
Janine Cossy
@ca
Janine Cossy
@da
Janine Cossy
@en
Janine Cossy
@es
Janine Cossy
@fr
Janine Cossy
@hu
Janine Cossy
@nb
Janine Cossy
@nl
Janine Cossy
@nn
P1006
P214
P244
P268
P269
P1006
P106
P1153
7102425595
P1559
Janine Cossy
@fr
P1580
P19
P2038
Janine_Cossy
P21
P213
0000 0001 1597 7082
P214
P2381
P244
nb2010015534