129777-96-4

Upstream product

• 76910-02-6 3-cyclopenten-1,1-dimethanol 
• 100-39-0 benzyl bromide 

Downstream Products

• 129778-04-7 (+/-)-(1α,2β)-2-<2-amino-6-chloro-9H-purin-9-yl>-4,4-bis(benzyloxymethyl)-1-cyclopentanol 
• 129778-03-6 (+/-)-(1α,2β)-2-<(2,5-diamino-6-chloro-4-pyrimidinyl)amino>-4,4-bis(benzyloxymethyl)-1-cyclopentanol 
• 129778-01-4 (+/-)-(1α,2β)-2-(6-chloro-9H-purin-9-yl)-4,4-bis(benzyloxymethyl)-1-cyclopentanol 
• 129778-00-3 (+/-)-(1α,2β)-2-<(5-amino-6-chloro-4-pyrimidinyl)amino>-4,4-bis(benzyloxymethyl)-1-cyclopentanol 
• 129777-99-7 (+/-)-2-amino-4,4-bis(benzyloxymethyl)-1-cyclopentanol 
• 129777-97-5 1,1-bis(benzyloxymethyl)-3,4-epoxycyclopentane 

Relevant academic research and scientific papers

Ru-catalyzed cyclization of terminal alkynals to cycloalkenes

Cycloalkenes can be efficiently prepared by a new Ru-catalyzed cyclization of terminal alkynals. Under appropriate conditions, cycloisomerizations to conjugated aldehydes may be observed. Both processes involve catalytic Ru vinylidenes. Copyright