84017-49-2

Upstream product

• 873-51-8 phenylborondichloride 

Downstream Products

• 89377-15-1 1-phenyl-2-borolene 
• 102634-85-5 (3-butenyl)methoxyphenylborane 
• 87882-93-7 η-benzene-η5-(1-phenylborole)ruthenium 
• 112198-52-4 {Ru(η6-C6Me6)(η5-C4H4BC6H5)} 
• 121545-38-8 bis{η5-(1-phenylborol)}nickel 
• 103652-93-3 tricarbonyl(η5-1-phenylborole)iron 
• 118657-21-9 μ-(η5-C4H4BPh){V(CO)4}2 
• 143446-96-2 cis-5-trichloromethyl-2-phenyl-4-vinyl-1,2-oxaborolane 
• 143446-90-6 cis-5-p-tolyl-2-phenyl-4-vinyl-1,2-oxaborolane 
• 143447-16-9 5-Benzhydrylidene-4-eth-(E)-ylidene-2-phenyl-[1,2]oxaborolane 
• 102764-66-9 N(CH₃)4⁽¹⁺⁾*(CH₂CHCHCH₂B)C₆H₅(C(CH₃)3)^(1-) = {N(CH₃)4}(CH₂CHCHCH₂B)C₆H₅(C(CH₃)3) 
• 143447-14-7 trans-5-methyl-2-phenyl-4-vinyl-1,2-oxaborolane 
• 143446-94-0 cis-5-methyl-2-phenyl-4-vinyl-1,2-oxaborolane 
• 143447-18-1 CC(CH₂)5CH(CHCH₂)CH₂B(C₆H₅)O 

Relevant academic research and scientific papers

EINE EINFACHE SYNTHESE VON 3-BOROLONEN. DIE DARSTELUNG VON 1-PHENYL-3-BOROLONEN

The reactions of (1,3-diene)magnesium addition compounds with boron halides provide a simple route to 3-borolenes. 1-Phenyl-3-borolene, its trimethylamine adduct and tetramethylammonium (1,1-diphenylborata-3-cyclopentene) are described in detail.