11-Deoxycorticosterone. The Aqueous Sulfuric Acid Hydrolysis of 21-Diazoprogesterone

1955 ◽  
Vol 77 (4) ◽  
pp. 1055-1056 ◽  
Author(s):  
Charles G. Salem ◽  
W. Werner Zorbach
1972 ◽  
Vol 50 (23) ◽  
pp. 3767-3779 ◽  
Author(s):  
Wayne Irvine Congdon ◽  
John Thomas Edward

The rates of hydrolysis of 22 1-acyl-2-thiohydantoins in aqueous sulfuric acid to give 2-thiohydantoin and a carboxylic acid have been determined. In 0–90% sulfuric acid, hydrolysis takes place by an A-2 mechanism, and the rate reaches a maximum in about 70% acid. In acid more concentrated than about 90%, hydrolysis takes place by an A-1 mechanism, and the rate increases monotonically. Evidence for the two mechanisms comes from Yates r and Bunnett-Olsen [Formula: see text] parameters; from entropies of activation; from pσ and pσ+ relations; and from steric effects.


2017 ◽  
Vol 39 (4) ◽  
pp. 423 ◽  
Author(s):  
George Meredite Cunha de Castro ◽  
Norma Maria Barros Benevides ◽  
Maulori Curié Cabral ◽  
Rafael De Souza Miranda ◽  
Enéas Gomes Filho ◽  
...  

 The seaweeds are bio-resource rich in sulfated and neutral polysaccharides. The tropical seaweed species used in this study (Solieria filiformis), after dried, shows 65.8% (w/w) carbohydrate, 9.6% (w/w) protein, 1.7% (w/w) lipid, 7.0% (w/w) moisture and 15.9% (w/w) ash. The dried seaweed was easily hydrolyzed under mild conditions (0.5 M sulfuric acid, 20 min.), generating fermentable monosaccharides with a maximum hydrolysis efficiency of 63.21%. Galactose and glucose present in the hydrolyzed were simultaneously fermented by Saccharomyces cerevisiae when the yeast was acclimated to galactose and cultivated in broth containing only galactose. The kinetic parameters of the fermentation of the seaweed hydrolyzed were Y(P⁄S) = 0.48 ± 0.02 g.g−1, PP = 0.27 ± 0.04 g.L−1.h−1, h = 94.1%, representing a 41% increase in bioethanol productivity. Therefore, S. filiformis was a promising renewable resource of polysaccharides easily hydrolyzed, generating a broth rich in fermentable monosaccharides for ethanol production. 


1985 ◽  
Author(s):  
John F. Harris ◽  
Andrew J. Baker ◽  
Anthony H. Conner ◽  
Thomas W. Jeffries ◽  
James L. Minor ◽  
...  

2007 ◽  
Vol 46 (7) ◽  
pp. 1938-1944 ◽  
Author(s):  
Eliana V. Canettieri ◽  
George J. M. Rocha ◽  
João A. Carvalho, ◽  
João B. A. Silva

2012 ◽  
Vol 4 (2) ◽  
pp. 021201 ◽  
Author(s):  
I. P. Hernández ◽  
José A. Pérez-Pimienta ◽  
Sarah Messina ◽  
Claudia E. Saldaña Durán

2013 ◽  
Vol 68 ◽  
pp. 372-378 ◽  
Author(s):  
Normah Bujang ◽  
Miradatul Najwa Muhd Rodhi ◽  
Mohibah Musa ◽  
Fuzieah Subari ◽  
Norazlina Idris ◽  
...  

2017 ◽  
Vol 95 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Djallila Missaoui ◽  
Ali Rahmouni ◽  
Okkacha Bensaid ◽  
Néji Besbes

Quantum chemical studies of the acid hydrolysis of cis-cis-N-benzoyl-9-azabicyclo[6.1.0]non-4-ene in gas phase and sulfuric acid solution have been carried out. Conformational analysis of reactant and intermediates were done at DFT level of calculations, using different basis sets. Transition states were identified and IRC calculations were done at the same level. In the first step of the reaction, the protonation occurs preferentially on the nitrogen atom. Three products are obtained. The type of mechanism, stepwise or concerted, depends on the stable conformers and the cleaved N–C bond. The main conclusion is that the products of the reaction depend on the nature of the stable conformer of the reactant.


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