877464-08-9

Upstream product

• 877464-09-0 (+)-(1R,5R,6S)-6-acetyl-8-benzyloxycarbonyl-8-azabicyclo[3.2.1]oct-3-en-2-one 
• 126-39-6 2-ethyl-2-methyl-1,3-dioxolane 
• 877464-10-3 (+)-(1R,5R,6S)-8-benzyloxycarbonyl-6-(1-methyl-1,1-dioxacyclopentyl)-8-azabicyclo[3.2.1]oct-3-en-2-one 

Downstream Products

• 877464-13-6 (-)-(1R,2S,5R,6S)-6-acetyloxy-8-benzyloxycarbonyl-8-azabicyclo[3.2.1]octan-2-ol 
• 877464-12-5 (+)-(1R,2S,5R,6S)-6-acetyl-8-benzyloxycarbonyl-8-azabicyclo[3.2.1]octan-2-ol 
• 877464-11-4 (-)-(1R,2S,5R,6S)-8-benzyloxycarbonyl-6-(1-methyl-1,1-dioxacyclopentyl)-8-azabicyclo[3.2.1]octan-2-ol 

Relevant academic research and scientific papers

Organometallic enantiomeric scaffolding: Organometallic chirons. Total synthesis of (-)-Bao Gong Teng A by a molybdenum-mediated [5+2] cycloaddition

Bao Gong Teng A, an optically active tropane alkaloid with hypotensive and miotic activity isolated from the Chinese herb Erycibe obtusifolia Benth, was synthesized by an "organometallic chiron" strategy in which single enantiomers of TpMo(CO)2