Boiling Points and Boiling Point Numbers of Alkyl Derivatives of Bivalent S, Se, and Te.

1964 ◽  
Vol 9 (2) ◽  
pp. 272-275 ◽  
Author(s):  
Herbert H. Anderson
1984 ◽  
Vol 49 (1) ◽  
pp. 313-319 ◽  
Author(s):  
Věra Přikrylová ◽  
Petr Sedmera ◽  
Josef V. Jizba ◽  
Jindřich Vokoun ◽  
Helena Lipavská ◽  
...  

Reaction of daunomycinone (I) with alcohols and p-toluenesulfonic acid produces a mixture (~3 : 1) of its (7S)- and (7R)-O-alkyl derivatives II-IX. According to the 1H NMR evidence, the alicyclic ring exists in the 9H8 conformation in (7R)-O-alkyl derivatives, on the contrary to (7S)-epimers and 7-epi-daunomycinone that adopt the 8H9 conformation.


Author(s):  
D.M. Beltukova ◽  
V.P. Belik ◽  
Y.N. Antonenko ◽  
A.A. Bogdanov ◽  
G.A. Korshunova ◽  
...  

1897 ◽  
Vol 21 ◽  
pp. 156-159
Author(s):  
Crum Brown ◽  
R. Fairbairn

Sodium mercaptide and dibromosuccinic ether, in the proportion of two molecules of the former to one of the latter, were dissolved separately in absolute alcohol, and slowly mixed. A considerable evolution of heat took place, while sodium bromide separated out. The flask was then digested for some hours on the steam-bath. The alcohol was subsequently distilled off, and the residue, on cooling, was treated with water. An oil separated out. This oil was collected by means of a separating funnel, and the aqueous layer several times extracted with ether. The oil and the ethereal extracts were added together and dried over calcium chloride. Next morning the ether was distilled off at the ordinary pressure. The remainder was distilled in vacuo. Between 50° and 60° a few drops came over, which proved to be ethyldisulphide.The remainder came over between 150° and 170°.This latter fraction was redistilled, and a portion of it used for analysis. The boiling point at 20 mm. pressure was 160°.Combustion of dietthiosuccinic ether.Weight of substance taken = ·2477 gram.Weight of carbonic acid obtained = ·4476 gram.Weight of water obtained = ·1702 gram.


1990 ◽  
Vol 9 (1) ◽  
pp. 260-265 ◽  
Author(s):  
Rocco A. Paciello ◽  
Juan M. Manriquez ◽  
John E. Bercaw

1933 ◽  
Vol 55 (11) ◽  
pp. 4657-4662 ◽  
Author(s):  
Emil Klarmann ◽  
Louis W. Gates ◽  
Vladimir A. Shternov ◽  
Philip H. Cox

Author(s):  
J. A. Barltrop ◽  
R. M. Acheson ◽  
P. G. Philpott ◽  
K. E. MacPhee ◽  
J. S. Hunt

Part I. — Pressures below 760 mm . In a previous communication (‘Proc.’, A, vol. 82, 1909, p. 396) the approximate boiling points of a number of metals were determined at atmospheric pressure. Apart from the question of finding the exact relation between the boiling point and pressure, it is an important criterion of any method for fixing the temperatures of ebullition to demonstrate that the experimental values obtained are dependent on the pressure. It is specially desirable when dealing with substances boiling at temperatures above 2000° to have some evidence that the points indicated are true boiling points. Previous work on the vaporisation of metals at different pressures has been confined to experiments in a very high vacuum except for metals like bismuth, cadmium, and zinc, which boil at relatively low temperatures under atmospheric pressure. The observations were limited to very low pressures on account of the difficulty of obtaining any material capable of withstanding a vacuum at temperatures over 1400° and the consequent necessity for keeping the boiling point below this limit by using very low pressures. Moreover in the case of the majority of the metals, e. g. , copper, tin, ebullition under reduced pressure has never been observed. The difficulties indicated above were avoided by using a similar type of apparatus to that previously described, and arranging the whole furnace inside a vacuum enclosure, thus permitting of the use of graphite crucibles to contain the metal.


1966 ◽  
Vol 44 (11) ◽  
pp. 1247-1258 ◽  
Author(s):  
Raj Nandan Prasad ◽  
Karin Tietje

The formation of 3-oxo-3,4-dihydro-2H-1,4-benzothiazine (IIIa) by cyclization of alkyl 2-haloacetamidophenyl sulfides (I) was investigated; it is proposed that the reaction proceeds via a six-membered sulfonium halide. The preparation of 4-alkyl derivatives of IIIa and of 4-alkyl and 4-acyl derivatives of its reduction product 3,4-dihydro-2H-1,4-benzothiazine (Va) is described. Acylation of Va was shown to proceed without opening of the thiazine ring. Preparation of the O-benzoyl, N-benzoyl, and O,N-dibenzoyl derivatives of 2-(β-hydroxyethyl-mercapto)aniline (VIII) has permitted clarification of the confusion in the literature with respect to the derivatives of Va and VIII. Compound XVIII, the 1,1-dioxide of IIIa, undergoes C-alkylation at the 2-position when treated with alkyl halides, rather than O-alkylation as previously suggested.


ARKIVOC ◽  
2022 ◽  
Vol 2022 (2) ◽  
Author(s):  
Shushanik Shamir Dashyan ◽  
Ruzanna Garnik Paronikyan ◽  
Suren Sergey Mamyan ◽  
Ervand Garnik Paronikyan

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