about
Copper-mediated aromatic amination reaction and its application to the total synthesis of natural products.Structural Determination of (-)-SCH 64874 and Hirsutellomycin by Semisynthesis.Total synthesis of dictyodendrin A and B.Enantiocontrolled total synthesis of (-)-mersicarpine.Generation of cycloalkynes through deprotonation of cyclic enol triflates with magnesium bisamides.Total synthesis of (+)-yatakemycin.One-Pot Halogen Dance/Negishi Coupling of Dibromothiophenes for Regiocontrolled Synthesis of Multiply Arylated Thiophenes.Ring-expansion reaction of oximes with aluminum reductants.Regiocontrolled Halogen Dance of Bromothiophenes and BromofuransA mild inter- and intramolecular amination of aryl halides with a combination of CuI and CsOAcSynthesis of secondary arylamines through copper-mediated intermolecular aryl aminationTotal synthesis of (+)-yatakemycinConcise total synthesis of (-)-mersicarpineTotal synthesis of dictyodendrins A-ETotal synthesis of (-)-acetylaranotinTotal synthesis of (-)-haouamine B pentaacetate and structural revision of haouamine BSynthetic studies toward penitrem E: enantiocontrolled construction of B-E ringsSynthesis of substituted indoline and carbazole by benzyne-mediated cyclization-functionalizationTotal Synthesis of (+)-MPC1001BSynthesis of Thieno[3,2-b]indoles via Halogen Dance and Ligand-Controlled One-Pot Sequential Coupling ReactionMagnesium Bisamide-Mediated Halogen Dance of BromothiophenesTotal Synthesis of (-)-Histrionicotoxin through a Stereoselective Radical Translocation-Cyclization ReactionUnprecedented Regioregular Poly(1,4-arylene)s Prepared by Nickel(II)-Catalyzed Cross-Coupling Polymerization of 2,5-Disubstituted Bromo(chloro)aryleneTotal Synthesis of (+)-CC-1065 Utilizing Ring Expansion Reaction of Benzocyclobutenone Oxime SulfonateNosyl (2-Nitrobenzenesulfonyl) Annulation Strategy toward Winding Vine-Shaped Bithiophenes
P50
Q38229059-F48F7F40-8D3A-431D-9C32-3A66C3608D4BQ39102334-F6492927-3D80-48F8-A779-26F3AFA3C89EQ42964835-C16FDD36-5C27-4B89-A42D-D96EE97C8546Q43957355-9CB544F5-A216-4E3F-B2B4-70556FBFEBC4Q46418171-D1C056A6-44A6-4BEB-B4D5-4448E0F56DEBQ46901277-0C85B923-EE55-41F5-A12D-7CC4B95919BCQ48255832-27973F5B-844E-47DB-B543-5C2D7FDE056FQ50509039-37D1BB6F-AC62-4FB2-A9E8-8031929CB082Q58617112-A63ED2F0-F9C3-4B78-9EB3-61F271672A74Q60120698-76F2F011-DAAA-405D-ABCA-E87B691D9FDFQ75187795-1A74F1B5-598B-4E3A-9F0B-E30B83147B73Q83874508-2BBAF827-2555-4EBD-A484-7747F639C4BAQ83920903-844D9CC9-7F35-4C23-AD57-EF5175787910Q85178375-7BE97E06-CCBC-46C1-9C00-A3024D81FD0BQ85477349-EF64B8B2-6AAB-49E6-83DD-9F6A412DBA00Q85682037-8FA8B94C-4F8B-460A-80C8-75F9BE453EF2Q86118500-CA051D10-C911-4E8A-8C68-05A70339434EQ86521392-83E95D1C-D530-4CFA-B0CC-77706195D2F2Q86541977-AF442684-1DF4-422D-BD3D-4F3E3FEBDBC2Q87728833-1D23BFA6-E5C2-4421-BF00-CC8747B9DD3EQ87989030-7CF87FE6-B3FA-4BA4-812C-F8C4F6EDFF31Q89010333-72D25FBE-C3BE-4EDB-9BC6-32713E54BFE9Q91880973-0136B93F-B3F2-4143-AA69-2E2936687FA4Q92678699-72D01AA8-77FA-443A-9B96-2C3F86060122Q93048027-6B396F2F-6F5A-480E-96B7-178D6D288983
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Kentaro Okano
@ast
Kentaro Okano
@en
Kentaro Okano
@es
Kentaro Okano
@nl
Kentaro Okano
@sl
type
label
Kentaro Okano
@ast
Kentaro Okano
@en
Kentaro Okano
@es
Kentaro Okano
@nl
Kentaro Okano
@sl
prefLabel
Kentaro Okano
@ast
Kentaro Okano
@en
Kentaro Okano
@es
Kentaro Okano
@nl
Kentaro Okano
@sl
P1053
J-8165-2014
P106
P21
P31
P3829
P496
0000-0003-2029-8505
P569
2000-01-01T00:00:00Z