173289-46-8

Upstream product

• 127299-55-2 (3R,4R)-3,4-bis(benzyloxy)pyrrolidine-2,5-dione 
• 87682-77-7 (Z)-4-(trimethylsilyl)-but-3-en-1-ol 

Downstream Products

• 173396-42-4 (4aS,6S,7S,7aS)-6,7-Bis-benzyloxy-5-eth-(Z)-ylidene-2,4a,5,6,7,7a-hexahydro-[1]pyrindine-1-carboxylic acid ethyl ester 
• 173289-51-5 (S)-6-((1S,2S)-1,2-Bis-benzyloxy-4,4-dibromo-but-3-enyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid ethyl ester 
• 173289-50-4 (S)-6-((1S,2R)-1,2-Bis-benzyloxy-3-oxo-propyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid ethyl ester 
• 173289-49-1 (1S,2R,8aS)-1,2-Bis-benzyloxy-1,5,6,8a-tetrahydro-2H-indolizin-3-one 
• 173289-52-6 (S)-6-((1S,2S)-1,2-Bis-benzyloxy-pent-3-ynyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid ethyl ester 
• 80152-07-4 (+)-streptazolin 

Relevant academic research and scientific papers

Stereoselective total synthesis of natural (+)-streptazolin via a palladium-catalyzed enyne bicyclization approach

The natural Z isomer of (+)-streptazolin (1), isolated from cultures of Streptomyces viridochromogenes, was synthesized in an optically pure form for the first time on the basis of a palladium-catalyzed enyne bicyclization approach in 12 steps and 4.3% ov