JP2009185063A5 - - Google Patents

Download PDF

Info

Publication number
JP2009185063A5
JP2009185063A5 JP2009120386A JP2009120386A JP2009185063A5 JP 2009185063 A5 JP2009185063 A5 JP 2009185063A5 JP 2009120386 A JP2009120386 A JP 2009120386A JP 2009120386 A JP2009120386 A JP 2009120386A JP 2009185063 A5 JP2009185063 A5 JP 2009185063A5
Authority
JP
Japan
Prior art keywords
reagent
organic synthesis
synthesis reaction
reaction
group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2009120386A
Other languages
English (en)
Japanese (ja)
Other versions
JP2009185063A (ja
JP5113118B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority to JP2009120386A priority Critical patent/JP5113118B2/ja
Priority claimed from JP2009120386A external-priority patent/JP5113118B2/ja
Publication of JP2009185063A publication Critical patent/JP2009185063A/ja
Publication of JP2009185063A5 publication Critical patent/JP2009185063A5/ja
Application granted granted Critical
Publication of JP5113118B2 publication Critical patent/JP5113118B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2009120386A 2006-03-24 2009-05-18 有機合成用試薬、及び当該試薬を用いた有機合成反応方法 Active JP5113118B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009120386A JP5113118B2 (ja) 2006-03-24 2009-05-18 有機合成用試薬、及び当該試薬を用いた有機合成反応方法

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2006084019 2006-03-24
JP2006084019 2006-03-24
JP2009120386A JP5113118B2 (ja) 2006-03-24 2009-05-18 有機合成用試薬、及び当該試薬を用いた有機合成反応方法

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2008511981A Division JPWO2007122847A1 (ja) 2006-03-24 2007-02-19 有機合成用試薬、及び当該試薬を用いた有機合成反応方法

Publications (3)

Publication Number Publication Date
JP2009185063A JP2009185063A (ja) 2009-08-20
JP2009185063A5 true JP2009185063A5 (https=) 2011-04-14
JP5113118B2 JP5113118B2 (ja) 2013-01-09

Family

ID=38624764

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2008511981A Pending JPWO2007122847A1 (ja) 2006-03-24 2007-02-19 有機合成用試薬、及び当該試薬を用いた有機合成反応方法
JP2009120386A Active JP5113118B2 (ja) 2006-03-24 2009-05-18 有機合成用試薬、及び当該試薬を用いた有機合成反応方法

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2008511981A Pending JPWO2007122847A1 (ja) 2006-03-24 2007-02-19 有機合成用試薬、及び当該試薬を用いた有機合成反応方法

Country Status (8)

Country Link
US (2) US8093435B2 (https=)
EP (1) EP2003104B1 (https=)
JP (2) JPWO2007122847A1 (https=)
CN (1) CN101405240B (https=)
AU (1) AU2007242276A1 (https=)
DK (1) DK2003104T3 (https=)
ES (1) ES2546808T3 (https=)
WO (1) WO2007122847A1 (https=)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2546808T3 (es) * 2006-03-24 2015-09-28 Jitsubo Co., Ltd. Reactivo para síntesis orgánica y método de reacción de síntesis orgánica con dicho reactivo
EP2415744A4 (en) 2009-03-12 2014-03-19 Ajinomoto Kk FLUORENE COMPOUND
WO2010113939A1 (ja) 2009-03-30 2010-10-07 味の素株式会社 ジフェニルメタン化合物
JP5803674B2 (ja) 2009-12-25 2015-11-04 味の素株式会社 ベンジル化合物
CN107011132B (zh) * 2010-08-30 2020-11-10 味之素株式会社 含有支链的芳香族化合物
CN103415530A (zh) 2011-03-09 2013-11-27 Jitsubo株式会社 新型的含有非肽性交联结构的交联肽、以及该交联肽的合成方法和用于该方法的新型有机化合物
JP5979139B2 (ja) 2011-05-17 2016-08-24 味の素株式会社 オリゴヌクレオチドの製造方法
JP6011528B2 (ja) 2011-05-31 2016-10-19 味の素株式会社 ペプチドの製造方法
WO2012165546A1 (ja) * 2011-05-31 2012-12-06 味の素株式会社 ペプチドの製造方法
CN102584546A (zh) * 2011-09-26 2012-07-18 盘锦兴福化工有限公司 2,3—二氟苯乙醚的合成方法
US9057712B1 (en) 2011-10-27 2015-06-16 Copilot Ventures Fund Iii Llc Methods of delivery of encapsulated perfluorocarbon taggants
EP2921499B1 (en) 2012-11-14 2020-01-22 Takeda Pharmaceutical Company Limited Method for liquid-phase synthesis of nucleic acids
US9504747B2 (en) 2013-03-08 2016-11-29 Novartis Ag Lipids and lipid compositions for the delivery of active agents
EP3608308B1 (en) 2013-03-08 2021-07-21 Novartis AG Lipids and lipid compositions for the delivery of active agents
WO2014189142A1 (ja) 2013-05-24 2014-11-27 味の素株式会社 モルフォリノオリゴヌクレオチドの製造方法
US9365615B2 (en) 2013-09-09 2016-06-14 Jitsubo Co., Ltd. Cross-linked peptides containing non-peptide cross-linked structure, method for synthesizing cross-linked peptides, and novel organic compound used in method
EP3263579B1 (en) 2015-01-21 2022-11-30 Ajinomoto Co., Inc. Precipitation promoter and precipitation method in which same is used
EP3266792B1 (en) * 2015-03-04 2020-12-30 Jitsubo Co., Ltd. Peptide synthesis method
KR101889893B1 (ko) * 2015-06-12 2018-08-22 애니젠 주식회사 선별적 용해도를 갖는 트리페닐메탄 유도체 및 그의 용도
KR102337328B1 (ko) 2015-12-21 2021-12-10 텍사스 테크 유니버시티 시스템 용액상 gap 펩타이드 합성을 위한 시스템 및 방법
US10981940B2 (en) 2016-11-11 2021-04-20 SEKISUl MEDICAL CO., LTD. Trityl protecting agent
EP3480195A1 (en) 2017-11-07 2019-05-08 Bayer Animal Health GmbH Method for the synthesis of cyclic depsipeptides
PL3676265T3 (pl) 2017-11-07 2025-12-15 Elanco Animal Health Gmbh Sposób syntezy cyklicznych depsypeptydów
EP3778621B1 (en) 2018-04-13 2023-08-23 Jitsubo Co., Ltd. Peptide synthesis method
US12024537B2 (en) 2018-05-31 2024-07-02 Sederma Compositions and methods for chemical synthesis
EP3882255A4 (en) 2018-11-16 2022-09-21 Ajinomoto Co., Inc. PROCESS FOR THE PREPARATION OF CYCLIZED PEPTIDE WITH INTRAMOLECULAR S-S BOND
EP3917937A4 (en) 2019-02-01 2022-11-23 Sederma SYNTHETIC STRATEGY FOR A SPLIT PROTECTION GROUP
JP7628073B2 (ja) 2019-02-28 2025-02-07 富士フイルム株式会社 ペプチド化合物の製造方法、保護基形成用試薬、及び、芳香族複素環化合物
JP7661880B2 (ja) 2019-04-25 2025-04-15 味の素株式会社 ペプチドの連続的製造方法
JP7301965B2 (ja) 2019-06-28 2023-07-03 富士フイルム株式会社 ペプチド化合物の製造方法、保護基形成用試薬、及び、縮合多環化合物
JP7814933B2 (ja) 2019-08-29 2026-02-17 富士フイルム株式会社 核酸化合物の製造方法、及び、核酸化合物
US20250282813A1 (en) 2021-04-09 2025-09-11 Bachem Holding Ag Pseudo solid phase protecting group and methods for the synthesis of oligonucleotides and oligonucleotide conjugates
JP7162853B1 (ja) 2021-07-02 2022-10-31 ペプチスター株式会社 液相ペプチド合成用担体結合ペプチドの分析方法
EP4596567A1 (en) 2022-11-01 2025-08-06 Chugai Seiyaku Kabushiki Kaisha Method for removing dibenzofulvene or dibenzofulvene derivative
JPWO2024143514A1 (https=) 2022-12-28 2024-07-04
EP4516392A1 (en) 2023-09-04 2025-03-05 Vito NV Peptides, peptidic nucleic acids (pna) and oligonucleotides synthesis assisted by membrane extraction
TW202542173A (zh) 2023-12-06 2025-11-01 美商安進公司 液相肽合成方法
CN119462823B (zh) * 2024-11-08 2025-11-11 西北工业大学 金团簇纳米酶配体和自组装水凝胶及水凝胶制备方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4014937A (en) * 1974-08-26 1977-03-29 Pfizer Inc. 3,4-And 3,5-dialkoxyphenethylamines
JPH06239995A (ja) * 1993-02-22 1994-08-30 Matsushita Electric Works Ltd ポリアニリン誘導体およびその製造方法
JP3919227B2 (ja) 1996-05-02 2007-05-23 テルモ株式会社 アミジン誘導体及びそれを構成成分とする薬物担体
JP2000044493A (ja) * 1998-07-27 2000-02-15 Asahi Chem Ind Co Ltd 化合物ライブラリー合成用保護基
JP2001122889A (ja) 1999-10-26 2001-05-08 Noguchi Inst 糖脂質アナログ化合物
US6806357B1 (en) 2001-08-20 2004-10-19 University Of Pittsburgh Fluorous nucleophilic substitution of alcohols and reagents for use therein
JP4283469B2 (ja) * 2001-12-19 2009-06-24 独立行政法人科学技術振興機構 相溶性−多相有機溶媒システムによりアミノ酸を逐次的に付加する液相ペプチド合成法
US20040214989A1 (en) * 2001-08-24 2004-10-28 Kazuhiro Chiba Compatible-multiphase organic solvent system
JP2003292494A (ja) 2002-04-01 2003-10-15 Japan Science & Technology Corp 温度依存的集合形態を有するデンドリマー及びそれから成る発光体
JP2004059509A (ja) 2002-07-30 2004-02-26 Nokodai Tlo Kk 液相ペプチド合成用アミノ酸試薬
WO2004073852A1 (ja) * 2003-02-24 2004-09-02 Tokyo University Of Agriculture And Technology Tlo Co., Ltd. 温度により相溶状態・分離状態が可逆変化する溶媒の組み合わせを用いた化学プロセス方法
JP4360854B2 (ja) 2003-07-08 2009-11-11 テルモ株式会社 グアニジン誘導体およびそれを構成成分とする薬物担体
JPWO2006104166A1 (ja) 2005-03-29 2008-09-11 国立大学法人東京農工大学 晶析分離用担体及び化合物の分離方法
ES2546808T3 (es) * 2006-03-24 2015-09-28 Jitsubo Co., Ltd. Reactivo para síntesis orgánica y método de reacción de síntesis orgánica con dicho reactivo

Similar Documents

Publication Publication Date Title
JP2009185063A5 (https=)
JP2010513498A5 (https=)
JP2008268931A5 (https=)
JP2009135422A5 (https=)
EP1927584A4 (en) BEAMER FOR SEPARATION, METHOD FOR SEPARATING A CONNECTION AND METHOD FOR SYNTHESIS OF A PEPTIDE USING THE SUPPORT
JP2008094844A (ja) ソリフェナシンの調製方法
Zhang et al. Palladium-catalyzed arene C–H activation/ketone C–H functionalization reaction: route to spirodihydroindenones
JP2011506531A5 (https=)
Nishimura et al. Synthesis of 4, 6-unsubstituted 2-aminodihydropyrimidine-5-carboxylates through sequential Staudinger/Aza-Wittig/cyclization reactions
JP2013521224A5 (https=)
Wang et al. Quinine/selectfluor combination induced asymmetric semipinacol rearrangement of allylic alcohols: an effective and enantioselective approach to α-quaternary β-fluoro aldehydes
CN101857559B (zh) 手性α-(三氯甲基)胺类化合物及其制备方法
JP2009137961A5 (https=)
WO2013121664A1 (ja) アセンジカルコゲノフェン誘導体用中間体及びその合成方法
Hasegawa et al. 2-Hydroxyphenyl-1, 3-dimethylbenzimidazolines. Formal two hydrogen atom-donors for photoinduced electron transfer reactions
Bolchi et al. Highly efficient resolutions of 1, 4-benzodioxane-2-carboxylic acid with para substituted 1-phenylethylamines
JP6224256B2 (ja) 放射ヨウ素標識された3−フルオロプロピル−NOR−β−CITの調製
JP2008526918A5 (https=)
Saha et al. Unified Synthesis of 10-Oxygenated Lycopodium Alkaloids: Impact of C10-Stereochemistry on Reactivity
Hu et al. Rhodium (III)‐Catalyzed Three‐Component Cascade Annulation for Modular Assembly of N‐Alkoxylated Isoindolin‐1‐Ones with Quaternary Carbon Center
JP2007048462A5 (https=)
CN102977127A (zh) 一种手性化合物
CN103965059A (zh) 一种制备(1r,2s)-2-(3,4-二氟苯基)环丙胺的方法
RU2014131118A (ru) Получение циклокарбонат-функционализованных соединений
Gontcharov et al. Development of a new practical synthesis of a 5-HT2C receptor agonist