JPH056538B2 - - Google Patents

Info

Publication number
JPH056538B2
JPH056538B2 JP63312373A JP31237388A JPH056538B2 JP H056538 B2 JPH056538 B2 JP H056538B2 JP 63312373 A JP63312373 A JP 63312373A JP 31237388 A JP31237388 A JP 31237388A JP H056538 B2 JPH056538 B2 JP H056538B2
Authority
JP
Japan
Prior art keywords
reaction
cyclohexyliminomethyl
isonitrile
pentane
ruthenium
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.)
Expired - Lifetime
Application number
JP63312373A
Other languages
English (en)
Japanese (ja)
Other versions
JPH02157253A (ja
Inventor
Teruyuki Hayashi
Masato Tanaka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP63312373A priority Critical patent/JPH02157253A/ja
Publication of JPH02157253A publication Critical patent/JPH02157253A/ja
Publication of JPH056538B2 publication Critical patent/JPH056538B2/ja
Granted legal-status Critical Current

Links

Classifications

    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
JP63312373A 1988-12-09 1988-12-09 シッフ塩基類の製造方法 Granted JPH02157253A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63312373A JPH02157253A (ja) 1988-12-09 1988-12-09 シッフ塩基類の製造方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63312373A JPH02157253A (ja) 1988-12-09 1988-12-09 シッフ塩基類の製造方法

Publications (2)

Publication Number Publication Date
JPH02157253A JPH02157253A (ja) 1990-06-18
JPH056538B2 true JPH056538B2 (enExample) 1993-01-26

Family

ID=18028475

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63312373A Granted JPH02157253A (ja) 1988-12-09 1988-12-09 シッフ塩基類の製造方法

Country Status (1)

Country Link
JP (1) JPH02157253A (enExample)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4572391B2 (ja) * 2006-01-11 2010-11-04 独立行政法人産業技術総合研究所 ビスホスフィノイルアミノメタン類の製造方法

Also Published As

Publication number Publication date
JPH02157253A (ja) 1990-06-18

Similar Documents

Publication Publication Date Title
Yamamoto Selective synthesis by use of Lewis acids in the presence of organocopper and related reagents. New synthetic methods (61)
Sato The preparation of Grignard reagents via the hydromagnesation reaction and their uses in organic synthesis
Song et al. Bis-paracyclophane N-heterocyclic carbene–ruthenium catalyzed asymmetric ketone hydrosilylation
Salem et al. Formation of Stable trans-Dihydride Ruthenium (II) and 16-Electron Ruthenium (0) Complexes Based on Phosphinite PONOP Pincer Ligands. Reactivity toward Water and Electrophiles
Breitenfeld et al. Why Are (NN2) Ni Pincer Complexes Active for Alkyl− Alkyl Coupling: β-H Elimination Is Kinetically Accessible but Thermodynamically Uphill
Luo et al. Fe-promoted cross coupling of homobenzylic methyl ethers with Grignard reagents via sp 3 C–O bond cleavage
Mauleón et al. Enantioselective construction of stereogenic quaternary centres via Rh-catalyzed asymmetric addition of alkenylboronic acids to α, β-unsaturated pyridylsulfones
Rappert et al. Synthesis and Properties of Cationic Hydrido (tertiary phosphine) ruthenium (II) Complexes
CN111420709B (zh) 氮杂环卡宾基混配型镍(ii)配合物在合成2-直链烷基苯并噻唑类化合物反应中的应用
Wallner et al. Palladium-catalyzed electrophilic substitution of allyl chlorides and acetates via bis-allylpalladium intermediates
Millan et al. Ti/Pd bimetallic systems for the efficient allylation of carbonyl compounds and homocoupling reactions
Inoue et al. Catalytic asymmetric Nozaki–Hiyama reactions with a tridentate bis (oxazolinyl) carbazole ligand
Zhou et al. Palladium-catalyzed 1, 4-addition of terminal alkynes to unsaturated carbonyl compounds promoted by electron-rich ligands
CN107915630A (zh) 一种琥珀酸二酯或琥珀酸二酯衍生物的制备方法
Dzhemilev et al. Some novelties in the chemistry of organomagnesium compounds with zirconium complexes
Bernard et al. Selectivity in carbon-oxygen bond formation: reaction of acid chlorides and methyl iodide with trans-(MeO) Ir (CO)(PPh3) 2
Mirza-Aghayan et al. Palladium catalyzed mild reduction of α, β-unsaturated compounds by triethylsilane
JPH056538B2 (enExample)
Akita et al. Deoxygenative Reduction of Diruthenium Carbonyl Complexes (η5-C5H4R) 2Ru2 (μ-CO) 2 (CO) 2 with Hydrosilanes Leading to Bridging Methylene Complexes (η5-C5H4R) 2Ru2 (μ-CH2) n (μ-CO) 2-n (CO) 2 (n= 1, 2; R= H, CH3)
Hyder et al. Nucleophilic Addition Reactions to Allenylidene Complexes of Ruthenium Bearing Hemilabile P, N Ligands: Isolation of the Vinylcarbene Complex [Cp* Ru CHCH CPh2 (iPr2PNHPy)][PF6]
Polm et al. Reactions of monoazadienes with metal carbonyl complexes III. Thermal conversion of n-alkyl-(e)-crotonaldimine with ru3 (co) 12 to σ-n, μ2-η3-allyl and μ2-η3-azaallyl bonded six electron fragments coordinated to a hexacarbonyl diruthenium unit. X-ray single crystal structure determinations of ru2 (co) 6 {σ-n, μ2-η3-ch2cc (h) c (h) n c4h9-t} and ru2 (co) 6 {μ2-η3-c2h5 cc (h) n c4h9−}
Arai et al. SN2'-Regio-and Diastereoselective Allylation of Organozinc Reagents.
JPH02219A (ja) 不飽和アルコールを製造する方法
Maruyama et al. Benzoyl (acetylacetonato) nickel (II) complexes containing tertiary phosphine ligands. Their synthesis, dynamic behavior in solution, and decarbonylation
Dash et al. Organoactinides—novel catalysts for demanding chemical transformations

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term