Mechanism of Hydrolysis of Hydroxy-alkane Sulfonic Acid Sultones

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Synthesis of Propyl-Sulfonic Acid-Functionalized Nanoparticles as Catalysts for Cellobiose Hydrolysis

Functionalization of silica surfaces using organo-silanes is highly sensitive to reaction conditions. Silica-coated nanoparticles were functionalized with propyl-sulfonic acid groups (PS) under different synthesis conditions including, various solvents (Ethanol, methanol, acetonitrile, and toluene), water content in the reaction media (0% to 50%), 3-mercaptopropyl-trimethoxysilane concentration...

متن کامل

On the mechanism of the acid-catalyzed hydrolysis of uridine to uracil. Evidence for 6-hydroxy-5,6-dihydrouridine intermediates.

In acidic media, the 5,6-double bond of uridine is rapidly hydrated to give a small amount of 6-hydroxy-5,6-dihydrouridine (Urd-H2O), the mechanism of which is known from studies of the acid-catalyzed dehydration of Urd-H2O (Prior, J. J., Maley, J., and Santi, D. V. (1984) J. Biol. Chem. 258, 2422-2428). In addition to dehydration, Urd-H2O also undergoes direct hydrolysis of the N-glycosidic bo...

متن کامل

Sulfonic Acid Group Functionalized Ionic Liquid Catalyzed Hydrolysis of Cellulose in Water: Structure Activity Relationships

Catalytic activities of eight sulfonic acid group functionalized ionic liquids in water were compared for the hydrolysis of Sigmacell cellulose (DP ~ 450) in the 150-180°C temperature range by measuring total reducing sugar (TRS) and glucose produced. The catalytic activity of acidic ionic liquids with different cation types decreases in the order imidazolium > pyridinium > triethanol ammonium ...

متن کامل

Stereoselectivity in the mechanism of acid hydrolysis of mitomycins.

predominance of the 1,2-cis-mitosene degradation products occurring at low pH was ascribed to the directing force exterted on the incoming nucleophile by the protonated 2-amino function of an intermediate in the process as well as to steric hindrance due to the orientation of the C9 urethane substituent in one of the degradation steps preceding the formation of the intermediate. The differences...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: The Journal of the Society of Chemical Industry, Japan

سال: 1971

ISSN: 0023-2734,2185-0860

DOI: 10.1246/nikkashi1898.74.4_715