160309-22-8

Upstream product

• 35166-78-0 cyclohexylmethyl magnesium bromide 
• 138913-30-1 (1R,4S,5S,6R)-3-chloro-4,5-O-isopropylidene-7-oxabicyclo[4.1.0]hept-2-ene-4,5-diol 
• 1078-58-6 diphenylzinc 
• 160309-17-1 (1R,4S,5S,6R)-3-chloro-4,5-(isopropylidenedioxy)-7-(4'-methylphenylsulfonyl)-7-azabicyclo<4.1.0>hept-2-ene 

Downstream Products

• 180165-13-3 (3aR,4S,5R,6S,7R,7aS)-5-Azido-6-cyclohexylmethyl-2,2-dimethyl-hexahydro-benzo[1,3]dioxole-4,7-diol 
• 180165-15-5 (3aR,4S,5R,6S,7R,7aS)-5-Amino-6-cyclohexylmethyl-2,2-dimethyl-hexahydro-benzo[1,3]dioxole-4,7-diol 
• 180165-11-1 (1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol 
• 180322-50-3 (3aS,4R,5S,7aR)-5-Cyclohexylmethyl-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-ol 

Relevant academic research and scientific papers

Oxa- and azabicyclo[4.1.0]heptenes as new synthons for C-disaccharide and alkaloid synthesis. Reactivity trends with carbon nucleophiles

Homochiral vinyloxiranes and vinylaziridines were reacted with a series of organometallic reagents in order to determine the regio- and stereoselectivity of the ring opening with carbon nucleophiles.

Toluene-dioxygenase-mediated cis-dihydroxylation of aromatics in enantioselective synthesis. Iterative glycoconjugate coupling strategy and combinatorial design for the synthesis of oligomers of nor-saccharides, inositols and pseudosugars with interesting

Vinyl epoxides 18 and 31 and vinylaziridines 24 and 25 derived from chloro- or bromocyclohexadiene-cis-diols 9 have been condensed with protected cyclitols 19, 37, and 46 in an iterative manner to generate dimeric, trimeric and tetrameric conduritol or am