Direct reduction of alcohols: highly chemoselective reducing system for secondary or tertiary alcohols using chlorodiphenylsilane with a catalytic amount of indium trichloride.
about
Stereoretentive chlorination of cyclic alcohols catalyzed by titanium(IV) tetrachloride: evidence for a front side attack mechanism.Total synthesis of taxane terpenes: cyclase phase.Site-selective catalysis of phenyl thionoformate transfer as a tool for regioselective deoxygenation of polyols.C3 -Symmetric Boron Lewis Acid with a Cage-Shape for Chiral Molecular Recognition and Asymmetric Catalysis.B(C6 F5 )3 -Catalyzed Chemoselective Defunctionalization of Ether-Containing Primary Alkyl Tosylates with Hydrosilanes.Reductive Amination/Cyclization of Keto Acids Using a Hydrosilane for Selective Production of Lactams versus Cyclic Amines by Switching of the Indium Catalyst.Chemoselective Silylative Reduction of Conjugated Nitriles under Metal-Free Catalytic Conditions: β-Silyl Amines and Enamines.Direct Substitution of Arylalkynyl Carbinols Provides Access to Diverse Terminal Acetylene Building Blocks.Copper-catalyzed reduction of alkyl triflates and iodides: an efficient method for the deoxygenation of primary and secondary alcohols.Potential Energy Surfaces for Reactions of X Metal Atoms (X = Cu, Zn, Cd, Ga, Al, Au, or Hg) with YH4 Molecules (Y = C, Si, or Ge) and Transition Probabilities at Avoided Crossings in Some CasesB(C6F5)3-katalysierte chemoselektive Defunktionalisierung von etherhaltigen primären Alkyltosylaten mit Hydrosilanen
P2860
Q36650713-08E95FE6-17DB-4825-8526-2430EC408818Q42164644-B27FA97C-498D-47BA-BA2F-045CF1DB82CDQ42934419-4B982EF3-E3E4-41AD-9DEF-5906ABD9EEB7Q48172345-AAFF8101-360D-4653-A738-22B039DDFA19Q48258429-6B478BB5-F55C-4EF1-BBA5-1452FB2064DBQ48277228-1CA345D5-4172-4972-8F64-F9F8791F7B06Q53222406-F4EAB199-0DF7-47EF-B8FA-CC596F0D5AA5Q53543284-C861C010-D48B-4E87-85D1-A44E0D674C97Q54488030-812C8D2A-B210-4DE0-8B4A-71A87F237717Q58699224-87504123-EED7-4EBE-AD5F-2C5D41830A82Q59203319-B48CA16F-A293-4069-A5CC-CBB177B97000
P2860
Direct reduction of alcohols: highly chemoselective reducing system for secondary or tertiary alcohols using chlorodiphenylsilane with a catalytic amount of indium trichloride.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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name
Direct reduction of alcohols: ...... amount of indium trichloride.
@en
Direct reduction of alcohols: ...... amount of indium trichloride.
@nl
type
label
Direct reduction of alcohols: ...... amount of indium trichloride.
@en
Direct reduction of alcohols: ...... amount of indium trichloride.
@nl
prefLabel
Direct reduction of alcohols: ...... amount of indium trichloride.
@en
Direct reduction of alcohols: ...... amount of indium trichloride.
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P2093
P356
P1476
Direct reduction of alcohols: ...... c amount of indium trichloride
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P2093
P304
P356
10.1021/JO0158534
P407
P577
2001-11-01T00:00:00Z