α-Amidinium Thiosulfates (Bunte Salts) as Antiradiation Drugs

1964 ◽  
Vol 7 (6) ◽  
pp. 766-768 ◽  
Author(s):  
Ludwig Bauer ◽  
Karen Rover Sandberg
Keyword(s):  
Bunte Salts

S-[(N-Terpenoid carboxamidinium)methyl] thiosulfates (Bunte salts) as potential antiradiation agents

1969 ◽  
Vol 47 (7) ◽  
pp. 1233-1237 ◽  
Author(s):  
Jerry M. Barton ◽  
Ludwig Bauer
Keyword(s):  
Bunte Salts

The synthesis of a number of α-acetamidinium Bunte salts, substituted on one of the nitrogen atoms by a terpenoid moiety, is reported.

Organic Thiosulfates (Bunte Salts):  Novel Surface-Active Sulfur Compounds for the Preparation of Self-Assembled Monolayers on Gold

Langmuir ◽  
1999 ◽  
Vol 15 (10) ◽  
pp. 3529-3537 ◽  
Author(s):  
Jukka Lukkari ◽  
Minna Meretoja ◽  
Ilkka Kartio ◽  
Kari Laajalehto ◽  
Markku Rajamäki ◽  
...  
Keyword(s):  
Sulfur Compounds ◽  
Self Assembled Monolayers ◽  
Assembled Monolayers ◽  
Surface Active ◽  
Self Assembled ◽  
Bunte Salts

Glycosyl Bunte Salts: A Class of Intermediates for Sugar Chemistry

2017 ◽  
Vol 20 (1) ◽  
pp. 76-79 ◽  
Author(s):  
Yasuhiro Meguro ◽  
Masato Noguchi ◽  
Gefei Li ◽  
Shin-ichiro Shoda
Keyword(s):  
Sugar Chemistry ◽  
Bunte Salts

Chlorolysis of Bunte Salts

2008 ◽  
pp. 1
Author(s):  
J. Drabowicz ◽  
P. Kiełbasiński ◽  
P. Łyżwa ◽  
A. Zając ◽  
M. Mikołajczyk
Keyword(s):  
Bunte Salts

ChemInform Abstract: Medium Effects in Unsymmetrical Disulfide Compounds: Synthesis from Bunte Salts.

ChemInform ◽  
2010 ◽  
Vol 26 (19) ◽  
pp. no-no
Author(s):  
P. HIVER ◽  
A. DICKO ◽  
D. PAQUER
Keyword(s):  
Medium Effects ◽  
Bunte Salts

A Novel Method for the Direct Synthesis of Symmetrical and Unsymmetrical Sulfides and Disulfides from Aryl Halides and Ethyl Potassium Xanthogenate

Synlett ◽  
2018 ◽  
Vol 29 (07) ◽  
pp. 986-992 ◽  
Author(s):  
M. Soleiman-Beigi ◽  
Z. Arzehgar
Keyword(s):  
Direct Synthesis ◽  
Aryl Halides ◽  
New Method ◽  
Alkyl Aryl ◽  
Novel Method ◽  
Aryl Sulfides ◽  
Bunte Salts

An efficient and new method for the synthesis of disulfides and sulfides via the reaction of aryl halides with ethyl potassium xanthogenate in the presence of MOF-199 is described. O-Ethyl-S-aryl ­carbonodithioate has a key role as an intermediate in this procedure; it was converted into symmetrical diaryl disulfides in DMF. Additionally, this could be applied to the synthesis of unsymmetrical aryl alkyl(aryl′) disulfides by the reaction with S-alkyl(aryl) sulfurothioates (Bunte salts) as well as unsymmetrical aryl alkyl(aryl′) sulfides in DMSO.

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