Triethylborane-induced radical reactions with gallium- and indium hydrides

[1]  B. Ranu,et al.  Use of indium hydride (Cl2InH) for chemoselective reduction of the carboncarbon double bond in conjugated alkenes , 2002 .

[2]  H. Yorimitsu,et al.  Trans-hydrometalation of alkynes by a combination of InCl3 and DIBAL-H: one-pot access to functionalized (Z)-alkenes. , 2002, Organic letters.

[3]  A. Baba,et al.  Remarkable Dependence of Diastereoselectivity on Anhydrous or Aqueous Solvent in the Indium Hydride Promoted Reductive Aldol Reaction of α,β-Unsaturated Ketones , 2002 .

[4]  A. Baba,et al.  Indium(III) chloride-sodium borohydride system: a convenient radical reagent for an alternative to tributyltin hydride system. , 2002, Journal of the American Chemical Society.

[5]  P. Renaud,et al.  Organoboranes as a source of radicals. , 2001, Chemical reviews.

[6]  A. Baba,et al.  Indium hydride: a novel radical initiator in the reduction of organic halides with tributyltin hydride , 2001 .

[7]  Tomoaki Nakamura,et al.  Reduction of Organic Halides with Tri-2-furylgermane: Stoichiometric and Catalytic Reduction , 2001 .

[8]  P. Renaud,et al.  Radicals in Organic Synthesis , 2001 .

[9]  Tomoaki Nakamura,et al.  Triethylborane-induced radical reaction with Schwartz reagent. , 2001 .

[10]  H. Shinokubo,et al.  Radical Reaction by a Combination of Phosphinic Acid and a Base in Aqueous Media , 2001 .

[11]  D. Jang,et al.  Facile synthesis of enantiopure (R)-malates , 2000 .

[12]  M. Yasuda,et al.  Selective reduction of acid chloride with a catalytic amount of an indium compound , 2000 .

[13]  Tomoaki Nakamura,et al.  Reduction of Organic Halides with Tri-2-Furanylgermane: Stoichiometric and Catalytic Reaction , 1999 .

[14]  O. Yamazaki,et al.  Tetraaryldisilanes as a novel strategic radical reagent , 1999 .

[15]  J. Walton,et al.  Flight from the Tyranny of Tin: The Quest for Practical Radical Sources Free from Metal Encumbrances. , 1998, Angewandte Chemie.

[16]  M. Yasuda,et al.  Preparation of a novel indium hydride and application to practical organic synthesis , 1998 .

[17]  O. Yamazaki,et al.  Novel Water-Soluble Organosilane Compounds as a Radical Reducing Agent in Aqueous Media , 1997 .

[18]  D. Crich,et al.  A Practical Method for the Removal of Organotin Residues from Reaction Mixtures. , 1996, The Journal of organic chemistry.

[19]  Sabine Hadida,et al.  Tris(2-(perfluorohexyl)ethyl)tin Hydride: A New Fluorous Reagent for Use in Traditional Organic Synthesis and Liquid Phase Combinatorial Synthesis , 1996 .

[20]  G. C. Fu,et al.  Organotin Hydride Catalyzed Carbon−Carbon Bond Formation: Radical-Mediated Reductive Cyclization of Enals and Enones , 1996 .

[21]  C. Chatgilialoglu,et al.  Tris(trimethylsilyl)germane as a Radical-Based Reducing Agent , 1995 .

[22]  B. Giese,et al.  Stereochemistry of Radical Reactions , 1995 .

[23]  M. Yamada,et al.  Selective reduction of organic compounds with indium hydride reagents , 1995 .

[24]  Wen Yang,et al.  A Nitrogen-Containing Stannane for Free Radical Chemistry , 1995 .

[25]  D. Barton,et al.  The invention of radical reactions. Part 32. Radical deoxygenations, dehalogenations, and deaminations with dialkyl phosphites and hypophosphorous acid as hydrogen sources , 1993 .

[26]  D. Kahne,et al.  Direct introduction of CH2OH by intermolecular trapping of CO , 1993 .

[27]  M. Lucarini,et al.  The trimethylsilyl substituent effect on the reactivity of silanes. Structural correlations between silyl radicals and their parent silanes , 1992 .

[28]  C. Chatgilialoglu Organosilanes as radical-based reducing agents in synthesis , 1992 .

[29]  D. Barton,et al.  Radical Deoxygenaton of Secondary and Primary Alcohols with Phenylsilane , 1991 .

[30]  W. Neumann,et al.  A polymer-supported organotin hydride and its multipurpose application in radical organic synthesis , 1991 .

[31]  H. Schaefer,et al.  Chlorogallanes (GaClH2, GaCl2H, and GaCl3) and Their Dimer Isomers , 1991 .

[32]  C. Willis,et al.  Radical chain reduction of alkyl halides, dialkyl sulphides and O-alkyl S-methyl dithiocarbonates to alkanes by trialkylsilanes , 1991 .

[33]  J. M. Simoes,et al.  Triphenylsilane : a useful radical-based reducing agent , 1990 .

[34]  D. Barton,et al.  An improved radical chain procedure for the deoxygenation of secondary and primary alcohols using diphenylsilane as hydrogen atom donor and triethylborane-air as initiator , 1990 .

[35]  C. Chatgilialoglu,et al.  Tris(alkylthio)silanes as New Reducing Agents via Radicals , 1990 .

[36]  D. Curran,et al.  Atom transfer cyclization reactions of .alpha.-iodo esters, ketones, and malonates: examples of selective 5-exo, 6-endo, 6-exo, and 7-endo ring closures , 1989 .

[37]  I. Boyer,et al.  Toxicity of dibutyltin, tributyltin and other organotin compounds to humans and to experimental animals. , 1989, Toxicology.

[38]  K. Oshima,et al.  New Method of Radical Formation , 1989 .

[39]  K. Nozaki,et al.  Et3B induced radical addition of Ph3SnH to acetylenes and its application to cyclization reaction , 1989 .

[40]  J. Hershberger,et al.  Evaluation of tributylgermanium hydride as a reagent for the reductive alkylation of active olefins with alkyl halides , 1988 .

[41]  W. Neumann Tri-n-butyltin Hydride as Reagent in Organic Synthesis , 1988 .

[42]  G. Stork,et al.  A catalytic tin system for trapping of radicals from cyclization reactions. Regio- and stereocontrolled formation of two adjacent chiral centers , 1986 .

[43]  J. Hershberger,et al.  Alkyl additions to active olefins by tributylgermanium hydride reduction of alkyl halides , 1985 .

[44]  B. P. Roberts,et al.  An E.S.R. study of the gallane radical anion , 1984 .

[45]  R. Mook,et al.  Free-radical cyclization of bromo acetals. Use in the construction of bicyclic acetals and lactones , 1983 .

[46]  Y. Ueno,et al.  Homolytic carbocyclization by use of a heterogeneous supported organotin catalyst. A new synthetic route to 2-alkoxytetrahydrofurans and .gamma.-butyrolactones , 1982 .

[47]  E. Corey,et al.  Method for catalytic dehalogenations via trialkyltin hydrides , 1975 .

[48]  H. Schmidbaur Heterosiloxanes and t‐Butoxy Compounds of Aluminum, Gallium, and Indium , 1965 .