Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Studies on Spiro Azetidinones and Spiro Thiazolidinones, III Synthesis of Some New Spiro Azetidinones, Spiro Thiazolidinones, Bis-azetidinones and Bis-thiazolidinones

View through CrossRef
Abstract Cyclocondensation reaction of 3-isatylideneoxime (1a), -hydrazone (1b), -phenyl-hydrazone (1c), semicarbazone (1d) and -thiosemicarbazone (1e) with chloroacetyl chloride (and thioglycolic acid) gave the corresponding spiro azetidinones (2) and spiro thiazolidinones (3). 3-Isatylidenehydrazone (1b) was condensed easily with aromatic aldehydes afforded a new 3-isatylidene azomethines (4) which submitted for cyclocondensation reaction with chloroacetyl chloride (and thioglycolic acid) giving bis-azetidinones (5) and bis-thiazolidinones (6), respectively.
Title: Studies on Spiro Azetidinones and Spiro Thiazolidinones, III Synthesis of Some New Spiro Azetidinones, Spiro Thiazolidinones, Bis-azetidinones and Bis-thiazolidinones
Description:
Abstract Cyclocondensation reaction of 3-isatylideneoxime (1a), -hydrazone (1b), -phenyl-hydrazone (1c), semicarbazone (1d) and -thiosemicarbazone (1e) with chloroacetyl chloride (and thioglycolic acid) gave the corresponding spiro azetidinones (2) and spiro thiazolidinones (3).
3-Isatylidenehydrazone (1b) was condensed easily with aromatic aldehydes afforded a new 3-isatylidene azomethines (4) which submitted for cyclocondensation reaction with chloroacetyl chloride (and thioglycolic acid) giving bis-azetidinones (5) and bis-thiazolidinones (6), respectively.

Related Results

Spiro: reshaping urban mobility across Africa
Spiro: reshaping urban mobility across Africa
Learning outcomes This case is designed to enable students to: Case overview/synopsis ...
Quinoline Based 2-Azetidinones, 4-Thiazolidinones and Their Potential Pharmacological Activities
Quinoline Based 2-Azetidinones, 4-Thiazolidinones and Their Potential Pharmacological Activities
Globally, many diseases with unmet therapeutic needs persist, including cancer, tuberculosis, and various infectious diseases. The rapid development of new drugs is crucial to coun...
Sorption Behaviors of Light Lanthanides(III) (La(III), Ce(III), Pr(III), Nd(III)) and Cr(III) Using Nitrolite
Sorption Behaviors of Light Lanthanides(III) (La(III), Ce(III), Pr(III), Nd(III)) and Cr(III) Using Nitrolite
The sorption of light lanthanides(III) (La(III), Ce(III), Pr(III), Nd(III)) and chromium(III) ions from acidic solutions on Nitrolite was studied at varying ions concentrations, pH...
Isolation, characterization and semi-synthesis of natural products dimeric amide alkaloids
Isolation, characterization and semi-synthesis of natural products dimeric amide alkaloids
 Isolation, characterization of natural products dimeric amide alkaloids from roots of the Piper chaba Hunter. The synthesis of these products using intermolecular [4+2] cycloaddit...
A Perspective on Arkansas Basin and Ozark Highland Prehistory
A Perspective on Arkansas Basin and Ozark Highland Prehistory
It is, from time to time, valuable to reassess and perhaps shed new light on long-held perspectives. In "The 'Northern Caddoan Area' was not Caddoan," Frank Schambach provides a pr...
A Practical Asymmetric Synthesis of Enantiopure Spiro[4,4]nonane‐1,6‐dione
A Practical Asymmetric Synthesis of Enantiopure Spiro[4,4]nonane‐1,6‐dione
AbstractA practical asymmetric synthesis of enantiopure spiro[4,4]nonane‐1,6‐dione, a valuable precursor for chiral ligand development, is reported. This synthetic strategy include...

Back to Top