188052-19-9

Upstream product

• 188052-17-7 (2'S)-1-methoxy-6-{[2'-(methoxymethyl)pyrrolidinyl]carbonyl}-1,4-cyclohexadiene 
• 102069-84-1 (S)-2-methoxy-1-[[2'-(methoxymethyl)pyrrolidinyl]carbonyl]benzene 

Downstream Products

• 188052-37-1 ((1S,6S)-6-Benzyloxy-1-methyl-cyclohex-2-enyl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone 
• 188052-23-5 ((1R,6S)-3-Benzenesulfonylmethyl-6-benzyloxy-1-methyl-cyclohex-2-enylmethoxy)-tert-butyl-dimethyl-silane 
• 188052-24-6 ((1R,6S)-3-Benzenesulfonylmethyl-6-benzyloxy-1-methyl-cyclohex-2-enyl)-methanol 
• 188052-25-7 (1S,6S)-3-Benzenesulfonylmethyl-6-benzyloxy-1-methyl-cyclohex-2-enecarbaldehyde 
• 188052-22-4 (1S,2S,3S,6R)-6-Benzenesulfonylmethyl-3-benzyloxy-2-hydroxymethyl-2-methyl-cyclohexanol 
• 188052-20-2 (1S,2S,5S,8S)-2-Benzyloxy-8-iodo-1-methyl-6-oxa-bicyclo[3.2.1]octan-7-one 
• 188052-21-3 ((1R,2R,3S,6S)-3-Benzyloxy-2-methyl-7-oxa-bicyclo[4.1.0]hept-2-yl)-methanol 

Relevant academic research and scientific papers

Enantioselective synthesis of a taxane C-ring component using the Schultz asymmetric Birch reduction methodology

The asymmetric Birch reduction methodology has been used to develop two complementary routes to the taxane C-ring component in an enantioenriched form.