Reversibility of electrochemical magnesium deposition from tetrahydrofuran solutions containing pyrrolidinyl magnesium halide

2011 ◽  
Vol 56 (18) ◽  
pp. 6530-6535 ◽  
Author(s):  
Qing Song Zhao ◽  
Yan Na NuLi ◽  
Yong Sheng Guo ◽  
Jun Yang ◽  
Jiu Lin Wang
Keyword(s):  
Magnesium Halide

Propane-1,3-di(magnesium halide)

1977 ◽  
Vol 99 (7) ◽  
pp. 2390-2391 ◽  
Author(s):  
Lawrence C. Costa ◽  
George M. Whitesides
Keyword(s):  
Magnesium Halide

scholarly journals Magnesium Halide Catalyzed anti-Aldol Reactions of Chiral N-Acylthiazolidinethiones.

ChemInform ◽  
2010 ◽  
Vol 33 (35) ◽  
pp. 28-28
Author(s):  
David A. Evans ◽  
C. Wade Downey ◽  
Jared T. Shaw ◽  
Jason S. Tedrow
Keyword(s):  
Aldol Reactions ◽  
Magnesium Halide

Silyl Derivatives of the Mixed Sandwiches Cyclopentadienyl Manganese Benzene and Cyclopentadienyl Manganese Biphenyl, CpMn(C6H6) and CpMn(C6H5-Ph)

1997 ◽  
Vol 52 (9) ◽  
pp. 1037-1042 ◽  
Author(s):  
Max Herberhold ◽  
Thomas Hofmann ◽  
Stefanie Weinberger ◽  
Bernd Wrackmeyer
Keyword(s):  
Nmr Spectroscopy ◽  
Membered Ring ◽  
Grignard Reagents ◽  
Sandwich Complexes ◽  
Subsequent Reaction ◽  
Silyl Derivatives ◽  
Magnesium Halide ◽  
Derivatives Of

Mixed manganese sandwich complexes containing a silyl-substituted cyclopentadienyl ring, e. g. (η5 - C5H4 - R)Mn(η6- C6H6) (3a - c) and (η5- C5H4 - R)Mn(η6- C6H5 - Ph) (4a - c); (R = SiMe3 (a), Si2Me5 (b) and SiMe2tBu (c)), were obtained in low yield via intermediates {(η5 - C5H4 - R)MnCl} and their reaction with phenyl Grignard reagents. Use of the 4-trimethylsilyl-phenyl magnesium halide in the reaction with the intermediate {CpMnCl} led to complexes with silylsubstituted arene rings, CpMn(η6 - C6H5 - R′) (5a) and CpMn(η6 -R′ - C6H5 - C6H5 - R′) (6a); (R′ = SiMe3 (a)). Dilithiation of CpMn6H6) (1) and subsequent reaction with a chlorosilane gave (η5-C5H4 - R)Mn(η6 - C6H5 - R′) (7a,b); (R = R′ = SiMe3 (a), Si2Me5 (b)). A cyclophane 8 in which five- and six-membered ring are linked through a -Me2Si-SiMe2- bridge was obtained using 1,2-dichloro-tetramethyldisilane. The mixed manganese sandw ich complexes were thoroughly characterized by 1H , 13C, 29Si and 55Mn NMR spectroscopy. The 55Mn spectra can be used to detect low-yield side-products.

Novel synthesis of 4-halo-3-hydroxy-2-pyrone: one pot rearrangement–cyclization reaction by magnesium halide

Tetrahedron ◽  
2005 ◽  
Vol 61 (9) ◽  
pp. 2541-2547 ◽  
Author(s):  
Takuzo Komiyama ◽  
Yutaka Takaguchi ◽  
Aider T. Gubaidullin ◽  
Vakhid A. Mamedov ◽  
Igor A. Litvinov ◽  
...  
Keyword(s):  
Cyclization Reaction ◽  
One Pot ◽  
Novel Synthesis ◽  
Magnesium Halide

Grignard Reaction of 2-Substituted-3-Cyanoquinolines

1985 ◽  
Vol 40 (7) ◽  
pp. 990-995 ◽  
Author(s):  
◽  
Balkrishen Bhat ◽  
A. P. Bhaduri
Keyword(s):  
Cyano Group ◽  
The Other ◽  
Magnesium Bromide ◽  
Grignard Reaction ◽  
Reaction Products ◽  
Grignard Reactions ◽  
Magnesium Halide ◽  
Activated Surface

Abstract Grignard reactions of 2-morpholino and 2-methylthio-3-cyanoquinoline, 2-chloro-3-cyanoquinoline, 2-chloro-3-cyano-6-methoxyquinoline and 2-chloro-3-cyano-7-methylquinoline with alkyl or aryl magnesium halides have been studied. It was found that 2-morpholino and 2-methylthio- 3-cyanoquinolines gave 1,4-addition products followed by rapid aromatisation. 2-Chloro-3- cyanoquinoline with alkyl magnesium halides furnished 1,4-addition products but with aryl magnesium halides 1,4- and 1,2-addition products were obtained. The cyano group of 4-aryl-2-chloro- 3-cyano-1,4-dihydroquinolines was found to participate in the Grignard reaction to yield 1,2- addition products. 2-Chloro-3-cyano-6-m ethoxyquinoline with alkyl and phenyl magnesium halides yielded exclusively 1,4-addition products. Similarly with p-m ethoxyphenyl magnesium bromide, 1,4-addition products were isolated which participated in the Grignard reaction to yield the expected adducts. Unlike the other chloroquinoline derivatives, 2-chloro-3-cyano-7-methylquinoline with alkyl magnesium halide formed 1 ,2-addition products but with aryl magnesium halides, 1,4-addition products were isolated. The 4-alkyl-2-chloro-3-cyano-l,4-dihydroquinolines were unstable as compared to their 4-aryl analogs. A couple of the Grignard reaction products were found to be unstable on activated surface.

ChemInform Abstract: Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones.

ChemInform ◽  
2010 ◽  
Vol 33 (26) ◽  
pp. no-no
Author(s):  
David A. Evans ◽  
Jason S. Tedrow ◽  
Jared T. Shaw ◽  
C. Wade Downey
Keyword(s):  
Aldol Reactions ◽  
Magnesium Halide

ChemInform Abstract: Synthesis of Tetrahydrofurans by Regio- and Stereoselective Cyclization of Epoxyalcohols Using Magnesium Halide.

ChemInform ◽  
2010 ◽  
Vol 33 (23) ◽  
pp. no-no
Author(s):  
Michinori Karikomi ◽  
Shigeru Watanabe ◽  
Yukino Kimura ◽  
Tadao Uyehara
Keyword(s):  
Magnesium Halide

ChemInform Abstract: Magnesium Halide-Promoted Ring-Opening Reaction of Cyclic Ether in the Presence of Phosphine Halide.

ChemInform ◽  
2016 ◽  
Vol 47 (2) ◽  
Author(s):  
Yu-Chang Chang ◽  
Chia-Ming Weng ◽  
Tanveer M. Shaikh ◽  
Fung-E Hong
Keyword(s):  
Ring Opening ◽  
Cyclic Ether ◽  
Ring Opening Reaction ◽  
Magnesium Halide
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