Reactivity of alicyclic 1,5,9-triketones toward five-, six-, and seven-membered rings in acidic medium. Stereochemistry of intramolecular cyclization products

2022 ◽  
Author(s):  
Taisia I. Akimova ◽  
Olga A. Soldatkina ◽  
Andrey V. Gerasimenko ◽  
Vyacheslav G. Savchenko ◽  
Alevtina A. Kapustina
Keyword(s):  
Intramolecular Cyclization ◽  
Acidic Medium

Concise Synthesis of GB22 by Endo-Selective Siloxycyclopropane Arylation

2019 ◽  
Author(s):  
Hannah E. Burdge ◽  
Takuya Oguma ◽  
Takahiro Kawajiri ◽  
Ryan Shenvi
Keyword(s):  
Intramolecular Cyclization ◽  
Cross Coupling ◽  
Building Blocks ◽  
Ring Expansion ◽  
Dual Catalysis ◽  
Acid Labile

<div><div><div><p>The first synthesis of GB22 was accomplished by a con- cise, modular route. Two building blocks converged in a novel sp3-sp2 attached-ring coupling that used Ir/Ni dual-catalysis to reverse the regioselectivity of siloxycy- clopropane arylation. This cross-coupling proved general to access β-substituted tetralones via ring-expansion of indanone-derived siloxycyclopropanes. The congested, bridging rings of the GB alkaloids were completed using an aluminum-HFIP complex that effected intramolecular cyclization of an acid-labile substrate.</p></div></div></div>

Concise Synthesis of GB22 by Endo-Selective Siloxycyclopropane Arylation

2019 ◽  
Author(s):  
Hannah E. Burdge ◽  
Takuya Oguma ◽  
Takahiro Kawajiri ◽  
Ryan Shenvi
Keyword(s):  
Intramolecular Cyclization ◽  
Cross Coupling ◽  
Building Blocks ◽  
Ring Expansion ◽  
Dual Catalysis ◽  
Acid Labile

<div><div><div><p>The first synthesis of GB22 was accomplished by a con- cise, modular route. Two building blocks converged in a novel sp3-sp2 attached-ring coupling that used Ir/Ni dual-catalysis to reverse the regioselectivity of siloxycy- clopropane arylation. This cross-coupling proved general to access β-substituted tetralones via ring-expansion of indanone-derived siloxycyclopropanes. The congested, bridging rings of the GB alkaloids were completed using an aluminum-HFIP complex that effected intramolecular cyclization of an acid-labile substrate.</p></div></div></div>

Ag (I) Catalyzed Oxidation of SO2 in Aqueous Solution Differing Effect of Benzoate Ions in Acidic Medium

2017 ◽  
Vol 7 (4) ◽  
Author(s):  
Arun Kumar Sharma ◽  
Pradeep Parasher ◽  
Rashmi Sharma ◽  
Davarakonda S.N. Prasad
Keyword(s):  
Aqueous Solution ◽  
Acidic Medium ◽  
Differing Effect ◽  
Catalyzed Oxidation

Hydrogenation of nitrogen oxide on platinum-carbon catalysts in acidic medium

1981 ◽  
Vol 46 (11) ◽  
pp. 2669-2675 ◽  
Author(s):  
Ivo Paseka
Keyword(s):  
Nitrogen Oxide ◽  
Acidic Medium ◽  
Diffusion Region ◽  
Acid Solutions ◽  
Experimental Conditions ◽  
Platinum Content ◽  
Kinetically Controlled ◽  
Partial Pressures ◽  
Carbon Catalysts

Hydrogenation of nitrogen oxide in acid solutions on Pt-C catalysts proceeds in dependence on experimental conditions either in purely diffusion region or in the diffusion and kinetically controlled region. The boundary between these two processes shifts to the higher ratio of NO to H2 partial pressures with increasing platinum content and decreasing intensity of agitation.

Kinetics of hydrolysis of peroxodisulphate ions in acidic medium to peroxomonosulphuric acid

1981 ◽  
Vol 46 (5) ◽  
pp. 1229-1236 ◽  
Author(s):  
Jan Balej ◽  
Milada Thumová
Keyword(s):  
Ionic Strength ◽  
Rate Constants ◽  
Acidic Medium ◽  
Measured Data ◽  
Molar Ratios ◽  
Starting Solution ◽  
Kinetics Of Hydrolysis ◽  
Rate Of Hydrolysis ◽  
Kinetics Of ◽  
Hydrolysis Of

The rate of hydrolysis of S2O82- ions in acidic medium to peroxomonosulphuric acid was measured at 20 and 30 °C. The composition of the starting solution corresponded to the anolyte flowing out from an electrolyser for production of this acid or its ammonium salt at various degrees of conversion and starting molar ratios of sulphuric acid to ammonium sulphate. The measured data served to calculate the rate constants at both temperatures on the basis of the earlier proposed mechanism of the hydrolysis, and their dependence on the ionic strength was studied.

Cyclopropyl→cyclobutyl rearrangement in intramolecular cyclization of 3,5-bridged B-secoandrostane-6,7(or 5,7)-diols and mass spectra of products

1982 ◽  
Vol 47 (8) ◽  
pp. 2280-2290 ◽  
Author(s):  
Helena Velgová ◽  
Jorga Smolíková ◽  
Antonín Trka ◽  
Antonín Vítek
Keyword(s):  
Intramolecular Cyclization ◽  
Mass Spectra ◽  
Acid Catalyzed

Acid-catalyzed intramolecular cyclization of 6,7-dihydroxy-3α,5-cyclo-6,7-seco-5α-androstan-17-one (VII), 5,7-dihydroxy-3,5-methylene-5,7-secoandrostan-17-one and 5,7-dihydroxy-3β,5-cyclo-5,7-seco-A-homo-5β-androstan-17-one (XIII) in benzene and dioxane was investigated. The main cyclization products were 3,5-methylene-6-oxaandrostan-17-one (I) and/or 3β,5-cyclo-6-oxa-A-homo-5β-androstan-17-one (VIII). In the case of VI and VII the ratio of I and VIII was solvent-dependent: in benzene more VIII was formed than in dioxane. The mass spectra of I and VIII were almost identical and corresponded to the structure VIII.

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