374686-17-6

Upstream product

• 79271-56-0 triethylsilyl trifluoromethyl sulfonate 
• 374686-15-4 (5S,6R,7S,8R)-6,7,8-Tris-benzyloxy-5-ethynyl-deca-1,9-dien-5-ol 
• 73111-58-7 2,3,4-tri-O-benzyl-5,6-dideoxy-D-xylo-hex-5-enose 
• 85716-43-4 methyl 6-deoxy-6-iodo-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 347897-59-0 (6R,7S,8R)-6,7,8-Tris-benzyloxy-deca-1,9-dien-5-one 

Downstream Products

• 920266-25-7 (4S,5R,6S,7R)-5,6,7-Tris-benzyloxy-4-but-3-enyl-4-triethylsilanyloxy-non-8-en-2-ynoic acid methyl ester 

Relevant academic research and scientific papers

An efficient construction of bicyclic systems containing a seven-membered ring by tandem ring-closing metathesis reactions of dienynes

Various (5-7) and (6-7) bicyclic dienes bearing quaternary methyl group and ester functionality have been synthesized from acyclic dienynes by tandem ring-closing metathesis (RCM) reaction. Epoxidation of these conjugated dienes led to bicyclic vinyl oxir

Synthesis of polyoxygenated bicyclic systems containing medium-sized rings from carbohydrates via tandem metathesis of dienynes.

[reaction: see text] Highly functionalized (5-7), (5-8), and (6-8) ring systems have been prepared from carbohydrates via tandem ring-closing metathesis of dienynes.