Analysis of liquid-propellant rocket engines designed by F. A. Tsander

The development of the oxygen-gasoline OR-2 engines and the oxygen-alcohol GIRD-10 rocket engine is described. A result of Tsander's rocket research was an engineering method for propellant calculation of oxygen-propellant rocket engines that determined the basic parameters of the engine and the structural elements

A simple two-step synthesis of 2-(alkylamino)-1-arylethanols, including racemic adrenaline, from aromatic aldehydes via 5-aryloxazolidines

Benzaldehydes react smoothly with nonstabilized azomethine ylides, generated in situ from sarcosine/formaldehyde or N-(methoxymethyl)-N- (trimethylsilylmethyl)benzylamine, to give 5-aryloxazolidines as intermediates. These were converted into 2-(alkylamino)-1-arylethanols in good yields by simple heating in methanol with hydrochloric acid, or by treatment with hydrazine hydrate in ethanol. © 2013 Elsevier Ltd. All rights reserved

A one-pot synthesis of tetrahydroisoquinolin-4-ols via a novel acid-catalyzed rearrangement of 5-aryloxazolidines

Benzaldehydes with electron-donating substituents react smoothly with a nonstabilized azomethine ylide derived from sarcosine and formaldehyde to form 5-aryloxazolidines as intermediates, which undergo rearrangement into 2-methyl-1,2,3,4-tetrahydroisoquinolin-4-ols in high yields by simple heating with hydrochloric acid. This one-pot synthesis of tetrahydroisoquinolines can be considered as a formal [3+3] cycloaddition of the azomethine ylide to the aromatic aldehyde. © 2013 Elsevier Ltd. All rights reserved

Reaction of 5-aryloxazolidines with arylmagnesium bromides as a new route to N-benzyl-β-hydroxyphenethylamines as starting materials for the preparation of 4-aryl-1,2,3,4-tetrahydroisoquinolines

Benzaldehydes react smoothly with the non-stabilized azomethine ylide derived from sarcosine and formaldehyde to form 5-aryloxazolidines as intermediates, which undergo ring-opening to give N-benzyl-β- hydroxyphenethylamines in good yields by the action of arylmagnesium bromides. Their subsequent acid-catalyzed cyclization into 4-aryl-1,2,3,4- tetrahydroisoquinolines was performed in moderate to good yields. © 2013 Elsevier Ltd. All rights reserved

Preliminary results of the Vega 1 and Vega 2 optical investigation of aerosol in the atmosphere of Venus at 30-60 KM

Aerosol concentration profiles were measured by an aerosol spectrometer above the landing sites of the Vega 1 and Vega 2 landers. Approximately the same altitude zones were found as in previous experiments: a three-layered basic cloud cover, an intermediate zone and subcloud haze. There were significant quantitative differences in the concentrations of particles, however, and especially in the spectra of their dimensions. Nightglow was found in the troposphere of Venus at a wavelength of about 1 micron. The backscatter coefficient and the extinction coefficient change very little between 32 and 63 km. Large numbers of submicron particles apparently exist in the atmosphere above the landing sites

Spectrophotometric experiment on the Verera-11 and Venera-12 descent vehicles: Some results of the analysis of the spectrum of the daytime sky of Venus

The spectra of the daytime sky of Venus were recorded on the Venera-11 and Venera-12 descent vehicles at various altitudes above the planet's surface, within the interval of 4500 to 12,000 Angstroms. The angular distribution of the brightness of the scattered radiation was recorded and the ratio of water and carbon dioxide were studied, with respect to the cloud cover boundaries

Results and interpretation of measurements of the light flux in the near-surface layer of the Venusian atmosphere

The characteristics of the field of radiation in the near surface layer of the atmosphere and on the surface of Venus are reported. Optical measurements made during the landing of the descent vehicles are described. The relief of the surface and the amount of dust on it are examined. The spectral relationship of the albedo of the soil and the light flux incident on the surface is discussed

Synthesis of benzopyranopyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylides with 3-substituted coumarins

A three-component reaction of 3-substituted coumarins with N-alkyl-α-amino acids and aldehydes gave 1-benzopyrano[3,4-c]pyrrolidines as a result of a 1,3-dipolar cycloaddition of an intermediate nonstabilized azomethine ylide at the double bond of the coumarin system in moderate to good yields. In most cases, high regio- and stereo-selectivity of the [3+2] cycloaddition was observed. © 2013 Elsevier Ltd. All rights reserved

Highly diastereoselective 1,3-dipolar cycloaddition of nonstabilized azomethine ylides to 3-nitro-2-trihalomethyl-2H-chromenes: Synthesis of 1-benzopyrano[3,4-c]pyrrolidines

Reactions of 3-nitro-2-trifluoro(trichloro)methyl-2H-chromenes, including 2-unsubstituted derivatives, with N-alkyl-α-amino acids (sarcosine, proline) and paraformaldehyde proceed diastereoselectively to give 1-benzopyrano[3,4-c]pyrrolidines in good yields as a result of a 1,3-dipolar cycloaddition of the intermediate nonstabilized azomethine ylide at the Δ3-bond of the chromene system. © 2013 Elsevier Ltd. All rights reserved