111679-75-5

Upstream product

• 93233-92-2 2-Bromo-5,5-dimethyl-hexa-2,3-diene 

Downstream Products

• 111680-07-0 (1-tert-Butyl-3-methyl-penta-1,2-dienyl)-benzene 
• 111680-05-8 (1-tert-Butyl-1-ethyl-but-2-ynyl)-benzene 
• 111680-06-9 (1,1-Di-tert-butyl-but-2-ynyl)-benzene 
• 111680-09-2 (1-tert-Butyl-3,4,4-trimethyl-penta-1,2-dienyl)-benzene 
• 111680-08-1 (1-tert-Butyl-3,4-dimethyl-penta-1,2-dienyl)-benzene 
• 111679-96-0 (1-tert-Butyl-1-isopropyl-but-2-ynyl)-benzene 
• 66294-45-9 (1-tert-Butyl-3-methyl-buta-1,2-dienyl)-benzene 
• 111679-79-9 (1-tert-Butyl-1-methyl-but-2-ynyl)-benzene 
• 33124-21-9 (R)-3,3-Dimethyl-2-phenyl-1-butanol 
• 13491-16-2 (R)-(-)-α-tert-butylphenylacetic acid 
• 93233-56-8 (R)-5,5-Dimethyl-4-phenyl-hexane-2,3-dione 
• 64-19-7 acetic acid 

Relevant academic research and scientific papers

STEREOCHEMISTRY OF THE SN2' DISPLACEMENT OF CHIRAL 1,3-DISUBSTITUTED BROMOALLENES TO FORM CHIRAL ACETYLENES

Optically active 1,3-disubstituted bromoallenes react with a variety of cuprate reagents preferentially is an SN2' fashion with very high anti selectivity.