111180-63-3

Upstream product

• 5664-20-0 vinylidenecyclohexane 
• 280-64-8 9-bora-bicyclo[3.3.1]nonane 
• 21205-91-4 9-borabicyclo[3.3.1]nonane dimer 

Downstream Products

• 122775-27-3 1-vinyl-1-(1-hydroxy-1-methylpent-4-en-1-yl)cyclohexane 
• 122775-25-1 1-deuterio-1-vinyl-cyclohexane 
• 122775-31-9 1-vinyl-1-{1-hydroxy-1-(2-methylcyclopent-1-en-1-yl)ethyl}cyclohexane 
• 111180-65-5 1-vinyl-1-(1-hydroxyethyl)cyclohexane 
• 122775-28-4 1-vinyl-1-(1-hydroxy-1-methylprop-2-en-1-yl)cyclohexane 
• 111180-66-6 1-vinyl-1-(1-hydroxycyclopent-1-yl)cyclohexane 
• 63922-92-9 1-vinyl-1-(1-hydroxy-1-methylethyl)cyclohexane 
• 111180-64-4 1-vinyl-1-(1-ethoxyvinyl)cyclohexane 
• 123299-63-8 1-vinyl-1-(1-hydroxybut-2-en-1-yl)cyclohexane (E) 
• 124910-53-8 Methyl-[2-methyl-1-(1-vinyl-cyclohexyl)-propyl]-amine; hydrochloride 
• 123846-46-8 4-(1-Vinyl-cyclohexyl)-heptane-4-thiol 
• 124910-55-0 Methyl-[thiophen-2-yl-(1-vinyl-cyclohexyl)-methyl]-amine; hydrochloride 
• 124910-54-9 Methyl-[3-methyl-1-(1-vinyl-cyclohexyl)-butyl]-amine; hydrochloride 
• 123846-47-9 1-Phenyl-1-(1-vinyl-cyclohexyl)-ethanethiol 

Relevant academic research and scientific papers

Preparation of 1-substituted 1-vinylcycloalkanes from 3,3-tetra- and 3,3-penta-methyleneallylboranes

The boranes I and II, obtained by hydroboration of 1,1-tetra- and 1,1-penta-methyleneallenes with 9-BBN, were used as key reactants in the synthesis of a series of unsaturated gem-substituted carbinols (VIIa-VIIg, Xa-Xc, and XII), as well as 1,1-divinylcy

ALLYBORANES - MOLECULAR DESIGN.

Some aspects of the construction of cyclic, cage, and acrylic organic and organoboron systems with the use of triallylborane and various new allylic boranes 1-7 are presented. All known allylborane reactions are classified into six patterns, and principle