Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: Role of intramolecular non-bonded S⋅⋅⋅O interactions

نویسندگان

  • Aleksandar Rašović
  • Peter J. Steel
  • Erich Kleinpeter
  • Rade Marković
چکیده

A new synthetic approach to 2,3-dihydro-4H-1,3-thiazine derivatives based upon reductive rearrangement of 1,2-dithiole-3-ylidene thiones has been developed. In turn, the 1,2-dithiole derivatives were prepared by an efficient, ring-opening-closing process of 2-alkylidene-4-oxothiazolidines, induced in the presence of Lawesson’s reagent by intramolecular non-bonded 1,5-type S⋅⋅⋅O interactions in the 4-oxothiazolidine precursors.

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Multicomponent reaction for the first synthesis of 2,2-dialkyl- and 2-alkyl-2-aralkyl-5,6-diaryl-2H-1,3-thiazines as scaffolds for various 3,4-dihydro-2H-1,3-thiazine derivatives.

A two-step sequence for the synthesis of various 3,4-dihydro-2H-1,3-thiazines is presented. In the first step, 2H-1,3-thiazines were prepared by a new multicomponent reaction (MCR). Starting from β-chlorovinyl aldehydes, this MCR offers an efficient and facile access to 2,2-dialkyl- and 2-alkyl-2-aralkyl-5,6-diaryl-2H-1,3-thiazines. The potential of these products in subsequent reactions was ve...

متن کامل

Chemo-/regioselective synthesis of 6-unsubstituted dihydropyrimidinones, 1,3-thiazines and chromones via novel variants of Biginelli reaction.

A novel and facile cascade Biginelli-like assembly employing enaminone, aldehyde and urea/thiourea has been developed, which provides a highly chemo- and regioselective synthesis of new dihydropyrimidinones, 1,3-thiazines and chromones by altering particular functional groups in the reactants.

متن کامل

Helical organization of chiral binaphthyl tetrathiafulvalene primary amides through hydrogen bonding interactions

Chiral tetrathiafulvalenes, (R) or (S), or racemic, (R,S), are obtained from a phosphite-mediated cross coupling reaction of a 1,3-dithiole-2-thione derivative bearing one binaphthol moiety, and are transformed into binaphthol-based tetrathiafulvalene ortho-diamides. The X-ray crystal structures of five intermediate chiral 1,3-dithiole-2-one and 1,3-dithiole-2-thione derivatives reveal the form...

متن کامل

Synthesis of 2,2′-(1,4-Phenylene)bis-3,4-dihydro-2H-1,3-thiazin-4-ones and their Facile Recyclization to 2,2′-(1,4-Phenylene)bis(pyrimidin-4-one) and/or 2,2′-(1,4-Phenylene)-bis-(thieno[2,3-d]pyrimidin-4(1H)-one) Derivatives

1,3-Thiazines are an important type of heterocycles showing a wide variety of pharmacological properties. Thus, 1,3-thiazine derivatives have recently been reported as cholecystokinin antagonists [1], antimycobacterial agents [2], cannabinoid receptor agonists [3], and inhibitors of NO synthase (NOS) [4], as antibacterial [5], antipyretic [6], anti-inflammatory [6, 7], analgesic [7], antitumor ...

متن کامل

A New synthesis of functionalized imidazo[2,1-b][1,3]thiazines with thiohydantoins, isocyanides and dialkyl acetylenedicarboxylates

The reaction of stoichiometric amounts of dialkyl acetylenedicarboxylates with alkyl isocyanides and 5,5-diaryl thiohydantoins in toluene and catalytic amount of p-TSA afforded imidazo[2,1-b][1,3]thiazines in good overall yields

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

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2006