JP2016536301A5 - - Google Patents

Download PDF

Info

Publication number
JP2016536301A5
JP2016536301A5 JP2016525574A JP2016525574A JP2016536301A5 JP 2016536301 A5 JP2016536301 A5 JP 2016536301A5 JP 2016525574 A JP2016525574 A JP 2016525574A JP 2016525574 A JP2016525574 A JP 2016525574A JP 2016536301 A5 JP2016536301 A5 JP 2016536301A5
Authority
JP
Japan
Prior art keywords
alkyl
hydrocarbon
chain
optionally
aromatic
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
JP2016525574A
Other languages
English (en)
Japanese (ja)
Other versions
JP6499646B2 (ja
JP2016536301A (ja
Filing date
Publication date
Priority claimed from EP20130189792 external-priority patent/EP2865684A1/en
Application filed filed Critical
Publication of JP2016536301A publication Critical patent/JP2016536301A/ja
Publication of JP2016536301A5 publication Critical patent/JP2016536301A5/ja
Application granted granted Critical
Publication of JP6499646B2 publication Critical patent/JP6499646B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016525574A 2013-10-22 2014-10-14 アルキンのルテニウム触媒トランス選択的ヒドロスズ化方法 Expired - Fee Related JP6499646B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP20130189792 EP2865684A1 (en) 2013-10-22 2013-10-22 Process for the ruthenium catalyzed trans-selective hydrostannation of alkynes
EP13189792.8 2013-10-22
PCT/EP2014/072068 WO2015059006A1 (en) 2013-10-22 2014-10-14 Process for the ruthenium catalyzed trans-selective hydrostannation of alkynes

Publications (3)

Publication Number Publication Date
JP2016536301A JP2016536301A (ja) 2016-11-24
JP2016536301A5 true JP2016536301A5 (https=) 2018-08-09
JP6499646B2 JP6499646B2 (ja) 2019-04-10

Family

ID=49484142

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016525574A Expired - Fee Related JP6499646B2 (ja) 2013-10-22 2014-10-14 アルキンのルテニウム触媒トランス選択的ヒドロスズ化方法

Country Status (8)

Country Link
US (1) US9556209B2 (https=)
EP (2) EP2865684A1 (https=)
JP (1) JP6499646B2 (https=)
CN (1) CN105940007B (https=)
CA (1) CA2928148C (https=)
DK (1) DK3060571T3 (https=)
ES (1) ES2659775T3 (https=)
WO (1) WO2015059006A1 (https=)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3438077A1 (en) * 2017-07-31 2019-02-06 Studiengesellschaft Kohle mbH Process for deoxyfluorination of phenols
CN116947915A (zh) * 2022-04-14 2023-10-27 北京理工大学 一种铝氢催化的乙烯基锡烷化合物的制备方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0826047B2 (ja) * 1994-03-22 1996-03-13 工業技術院長 ビニルスタナン類の製造方法
US20080300288A1 (en) * 2005-06-30 2008-12-04 Purdue Research Foundation Alkenyldiarylmethanes, Fused Analogs And Syntheses Thereof

Similar Documents

Publication Publication Date Title
KR102338544B1 (ko) 실릴렌 리간드를 가지는 신규한 촉매
Leis et al. Cycloheptatrienyl, alkyl and aryl PCP-pincer complexes: Ligand backbone effects and metal reactivity
Strelnik et al. The assembly of unique hexanuclear copper (I) complexes with effective white luminescence
Berenguer et al. Facile metalation of Hbzq by [cis-Pt (C6F5) 2 (thf) 2]: a route to a pentafluorophenyl benzoquinolate solvate complex that easily coordinates terminal alkynes. Spectroscopic and optical properties
Bezkishko et al. Alkali and transition metal phospholides
Li et al. Copper‐Catalyzed Propargylic Substitution of Dichloro Substrates: Enantioselective Synthesis of Trisubstituted Allenes and Formation of Propargylic Quaternary Stereogenic Centers
JP2013102146A5 (ja) 化合物
JP2012134509A5 (https=)
Lawson et al. The carboboration of Me 3 Si-substituted alkynes and allenes with boranes and borocations
JP2012528811A5 (https=)
JP5999596B2 (ja) カルボジイミド化合物の製造方法
JP2019510760A5 (https=)
Müller et al. Tris (pyrazolyl) methanides of the alkaline earth metals: influence of the substitution pattern on stability and degradation
JP2016536301A5 (https=)
EP3186262A1 (en) Fluorosilicon nitrile compounds
Crespo et al. Reactions of [C, N, N′]-cyclometallated platinum compounds with phosphines: transphobia and effect of the chloro substituents: Crystal structure of [PtCl (3, 5-C6H2Cl2CHNCH2CH2NMe2)(PPh3) 2]
Naka et al. Catalytic deprotonative functionalization of propargyl silyl ethers with imines
Perekalin et al. Synthesis of the half-sandwich ruthenium complexes [Cp* RuL 3]+ via naphthalene replacement in [Cp* Ru (C 10 H 8)]+
Kläring et al. Insertion of CS2 into Iridium–Fluorine Bonds
Neogi et al. Regiospecific C (naphthyl)–H bond activation by platinum (II): Isolation, characterization, reactivity and TD-DFT study of the platinum (II) and platinum (IV) organometallates having [C, N, S] donor set
RU2017103477A (ru) Пиридиновый комплекс циркония, каталитическая система, включающая указанный пиридиновый комплекс циркония, и способ (со)полимеризации сопряженных диенов
JP2022022505A (ja) アルキニルシランの製造方法
CN102985431B (zh) 光学活性的1,2-双(二烷基膦)苯衍生物的制造方法
Crespo et al. Cyclometallated platinum compounds with chiral imines. Crystal structure of [PtMe (2-FC6H3CH N-(S)-CHMePh)(PPh3)]
Bartok et al. New silyl-substituted phosphaalkenes Mes* PC (Cl)–Si (Cl) PhR, promising building blocks in silicon and phosphorus chemistry