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https://doi.org/10.3390/chemistry6040034","","001305139700001","https://ousar.lib.okayama-u.ac.jp/67611","10.3390/chemistry6040034" "Keisuke;Tokushige|Takumi;Abe|","Formal One Carbon Deletion of Indoline Hemiaminals under Tautomeric Control to Access 2-Aminobenzyl Compounds","The Journal of Organic Chemistry","0022-3263","2024-07-01","89","14","10349","10354","isVersionOf https://doi.org/10.1021/acs.joc.4c00884","38949244","001261315500001","https://ousar.lib.okayama-u.ac.jp/67497","10.1021/acs.joc.4c00884" "Toshiki;Yamashiro|Takumi;Abe|","Switchable synthesis of 3-aminoindolines and 2′-aminoarylacetic acids using Grignard reagents and 3-azido-2-hydroxyindolines","Chemical Communications","1359-7345","2024","","","","","isVersionOf https://doi.org/10.1039/d4cc01448k","38847113","001240225400001","https://ousar.lib.okayama-u.ac.jp/67223","10.1039/d4cc01448k" "Takumi;Abe|","Synthetic strategies for the construction of C3–N1′ bisindoles","Organic and Biomolecular Chemistry","1477-0520","2024","22","9","1756","1764","isVersionOf https://doi.org/10.1039/d3ob02089d","38319400","001156670800001","https://ousar.lib.okayama-u.ac.jp/66645","10.1039/d3ob02089d" "Keisuke;Tokushige|Takumi;Abe|","On Demand Synthesis of C3−N1’ Bisindoles by a Formal Umpolung Strategy: First Total Synthesis of (±)‐Rivularin A","Chemistry – A European Journal","0947-6539","2024-01-08","30","11","e202302963","","isVersionOf https://doi.org/10.1002/chem.202302963","37988219","001142083100001","https://ousar.lib.okayama-u.ac.jp/66541","10.1002/chem.202302963" "Momoko;Kimata|Takumi;Abe|","Total Synthesis of the Proposed Structure of Indolyl 1,2-Propanediol Alkaloid, 1-(1H-Indol-3-yloxy)propan-2-ol","Chemistry","2624-8549","2023-12-12","5","4","2772","2784","isVersionOf https://doi.org/10.3390/chemistry5040177","","001132478200001","https://ousar.lib.okayama-u.ac.jp/66495","10.3390/chemistry5040177" 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Sciences","1422-0067","2023-02-23","24","5","4411","","","","","https://ousar.lib.okayama-u.ac.jp/64384","10.3390/ijms24054411" "Takumi;Abe|Ren;Nakajima|Toshiki;Yamashiro|Daisuke;Sawada|","First Total Synthesis of Reassigned Echinosulfonic Acid D","Journal of Natural Products","0163-3864","2022-08-17","85","8","2122","2125","isVersionOf https://doi.org/10.1021/acs.jnatprod.2c00559","35976728","000843929600001","http://escholarship.lib.okayama-u.ac.jp/63881","10.1021/acs.jnatprod.2c00559" "Takumi;Abe|Toshiki;Yamashiro|Kaho;Shimizu|Daisuke;Sawada|","Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines","Chemistry – A European Journal","0947-6539","2022-05-19","28","37","e202201113","","isVersionOf https://doi.org/10.1002/chem.202201113","35438809","000797645300001","http://escholarship.lib.okayama-u.ac.jp/63526","10.1002/chem.202201113" "Toshiki;Yamashiro|Takumi;Abe|Daisuke;Sawada|","Synthesis of 2-monosubstituted indolin-3-ones by cine-substitution 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