Can You Really Do Chemisty Experiments About 16400-32-1

Although many compounds look similar to this compound(16400-32-1)Computed Properties of C5H7Br, numerous studies have shown that this compound(SMILES:CCC#CCBr), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 16400-32-1, is researched, SMILESS is CCC#CCBr, Molecular C5H7BrJournal, Advanced Synthesis & Catalysis called Metal-Free, Base-Promoted, Tandem Pericyclic Reaction: A One-Pot Approach for Cycloheptane-Annelated Chromones from γ-Alkynyl-1,3-Diketones, Author is Liang, Yi-En; Kan, Chih-Yu; Barve, Balaji D.; Kuo, Yao-Haur; Fang, Hsu-Wei; Li, Wen-Tai, the main research direction is cycloheptachromone preparation; alkynyl diketone methoxyphenyl preparation intramol pericyclization.Computed Properties of C5H7Br.

A microwave-assisted, base-promoted tandem cyclization reaction strategy has been developed for the synthesis of cyclohepta[b]chromones I (R1 = H, Me, MeO, Cl, Ph, 4-MeOC6H4; R2 = H, Me, MeO; R3 = H; R2R3 = CH:CHCH:CH; R4 = H, Me, Et; R5 = H; R6 = H, Me, n-Pr, cyclopropyl, n-hexyl) and spiro cyclohepta[b]chromones I [R1 = H, Cl, Me, 4-MeC6H4O; R2 = H, Me, MeO; R3 = H; R4R5 = (CH2)3, (CH2)4, (CH2)5; R6 = H, Me]. Readily accessible γ-alkynyl-1,3-diketones II (X = MeO, Cl, Br, I) underwent intramol. cyclization and 7-endo-trig carbocyclization to afford various cycloheptane-annelated chromones I in one-pot reactions. This metal-free protocol also led to the generation of polycyclic ring with a new C-C bond and a new C-O bond.

Although many compounds look similar to this compound(16400-32-1)Computed Properties of C5H7Br, numerous studies have shown that this compound(SMILES:CCC#CCBr), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics