ChemInform Abstract: Reactions of 2-Substituted 3-Phenylpropenoyl Isothiocyanates with Sodium Hydrogen Sulfide.

ChemInform ◽  
1990 ◽  
Vol 21 (50) ◽  
Author(s):  
M. DZURILLA ◽  
P. KUTSCHY ◽  
D. KOSCIK ◽  
V. FICERI ◽  
R. KRAUS
Keyword(s):  
Hydrogen Sulfide ◽  
Sodium Hydrogen

Sodium Hydrogen Sulfide

2007 ◽  
pp. 128-131 ◽  
Author(s):  
Richard E. Eibeck ◽  
Ralph A. Zingaro ◽  
Raymond E. Mcglothlin
Keyword(s):  
Hydrogen Sulfide ◽  
Sodium Hydrogen

9-Oxobenzomorphans. IV. 9-Oxo-5-[3″-(1″-hydroxypropyl)]- and 9-oxo-5-[3″-(1″-sulfidrylpropyl)]-6,7-benzomorphans as cyclic hemiketals and hemithioketals

1981 ◽  
Vol 59 (2) ◽  
pp. 321-325 ◽  
Author(s):  
Gerry Kavadias ◽  
Stephan Velkof
Keyword(s):  
Hydrogen Sulfide ◽  
Sodium Hydroxide ◽  
Sodium Hydrogen

The syntheses of 9-oxobenzomorphans 10 and 12 are described. Both products exist in the cyclic forms 11 and 13 respectively. Hydrobromide and oxalate salts of the 9-oxobenzomorphan 1 when crystallized from methanol form stable methylhemiketals 4 and 5. Bromination of 5 yielded benzomorphan 8 which on treatment with sodium hydroxide produced, via 10, the cyclic hemiketal 11. Reaction of 8 with sodium hydrogen sulfide afforded, via 12, the cyclic hemithioketals 13.

Assessment of the effect of sodium hydrogen sulfide (hydrogen sulfide donor) on cisplatin-induced testicular toxicity in rats

2020 ◽  
Vol 27 (8) ◽  
pp. 8119-8128
Author(s):  
Nastaran Azarbarz ◽  
Zeinab Shafiei Seifabadi ◽  
Maasoumeh Zare Moaiedi ◽  
Esrafil Mansouri
Keyword(s):  
Hydrogen Sulfide ◽  
Testicular Toxicity ◽  
Sodium Hydrogen

ChemInform Abstract: Addition-Cyclization Reactions of Hexa-2,4-dienoyl Isothiocyanate with Amines and Sodium Hydrogen Sulfide.

ChemInform ◽  
2010 ◽  
Vol 31 (10) ◽  
pp. no-no
Author(s):  
M. Ruzinsky ◽  
M. Dzurilla ◽  
P. Kutschy ◽  
V. Kovacik
Keyword(s):  
Hydrogen Sulfide ◽  
Cyclization Reactions ◽  
Sodium Hydrogen

145 HNaS Sodium hydrogen sulfide

2014 ◽  
pp. 176-176
Author(s):  
E. Hirota ◽  
K. Kuchitsu ◽  
T. Steimle ◽  
J. Vogt ◽  
N. Vogt
Keyword(s):  
Hydrogen Sulfide ◽  
Sodium Hydrogen

scholarly journals Synthesis of fluorescent long-chain thiols/disulfides as building-blocks for self-assembled monolayers preparation

2012 ◽  
Vol 10 (2) ◽  
pp. 295-299 ◽  
Author(s):  
Sushilkumar Jadhav
Keyword(s):  
Hydrogen Sulfide ◽  
Nitrogen Heterocycles ◽  
Building Blocks ◽  
Self Assembled Monolayers ◽  
Sodium Hydrogen ◽  
End Groups ◽  
Assembled Monolayers ◽  
Self Assembled ◽  
Symmetrical Disulfides ◽  
Long Chain

AbstractNew symmetrical disulfides together with the corresponding thiols bearing fluorescent end-groups have been synthesized as building-blocks for self-assembled monolayers (SAMs). The synthesis has been accomplished starting from aromatic nitrogen heterocycles in three steps. The conversion of the tosylated intermediate into the final disulfide is accomplished by use of sodium hydrogen sulfide (NaSH). Both products (thiols and disulfides) were isolated and characterized.

Sign in / Sign up

Export Citation Format

Share Document