50484-00-9

Upstream product

• 4524-93-0 Cyclopentanecarboxylic acid chloride 
• 124-40-3 dimethyl amine 
• 822-87-7 2-Chlorocyclohexanone 
• 71473-74-0 6-chloro-N,N-dimethylhexanamide 
• 3400-45-1 cyclopentanecarboxylic acid 

Downstream Products

• 71364-50-6 N,N-dimethylcyclopent-1-ene-1-carboxamide 
• 1528-30-9 methylenecyclopentane 
• 21727-39-9 cyclopentylmethyltrimethylammonium iodide 
• 122687-60-9 2-phenyl-3-thia-1-azaspiro[4,4]non-1-ene-4-thione 

Relevant academic research and scientific papers

Vinyl-λ3-iodanes act as efficient sulfur atom acceptors: Vinylic SN2-based strategy for conversion of tertiary thioamides to amides

Exposure of tertiary thioamides to (E)-1-hexenyl(phenyl)-λ3-iodane results in vinylic SN2 reaction to give the inverted (Z)-S-vinylthioimidonium salts, which under alkaline hydrolysis (Na2CO3 or K2CO

218. Hetero-Diels-Alder Reaction with 1,3-thiazol-5(4H)-Thiones

On heating in toluene to 180 deg and on treatment with BF3*Et2O in CH2Cl2 at room temperature, 1,3-dienes react with the C=S group of 1,3-thiazol-5(4H)-thiones 1 in a reversible Diels-Alder reaction to give spiroheterocycles of type 6.A 1:1 mixture of two regioisomeric cycloadducts is formed in the thermal reaction with 2-methylbuta-1,3-diene (isoprene, 5b).In contrast, the formation of one regioisomer is strongly preferred in the BF3-catalyzed reaction.Frontier-orbital control as well as steric factors seem to be responsible for the observed regioselectivity.BF3-Catalyzed, cyclic 1,3-dienes and 1 also undergo a smooth Diels-Alder reaction.Whereas cyclohexa-1,3-diene (5c) reacts with 1a and 1b to give a single isomer (presumably the 'exo'-adduct), cyclopenta-1,3-diene (5d) leads to a ca. 3:1 mixture of 'exo'- and 'endo'-isomer.