137759-59-2

Upstream product

• 137759-57-0 Acetic acid (1R,2R,3R)-2-acetoxy-3-benzyloxy-1-((R)-1-benzyloxy-3,3-dimethoxy-propyl)-5,5-dimethoxy-pentyl ester 
• 137759-58-1 (3R,4S,5S,6R)-3,6-Bis-benzyloxy-1,1,8,8-tetramethoxy-octane-4,5-diol 
• 145332-78-1 Acetic acid (1R,2R,3R)-2-acetoxy-3-benzyloxy-1-((R)-1-benzyloxy-3-oxo-propyl)-5-oxo-pentyl ester 
• 137759-56-9 Acetic acid (1R,2R,3R)-2-acetoxy-3-benzyloxy-1-((R)-1-benzyloxy-but-3-enyl)-hex-5-enyl ester 
• 137759-54-7 (4R,5R)-4,5-Bis-((R)-1-benzyloxy-but-3-enyl)-2,2-dimethyl-[1,3]dioxolane 
• 145308-09-4 (4R,5S,6S,7R)-4,7-bis(benzyloxy)deca-1,9-diene-5,6-diol 
• 558-13-4 carbon tetrabromide 
• 137780-96-2 (R) 2-benzyloxy-4,4-dimethoxybutanal 

Downstream Products

• 145313-84-4 (Z)-7-[(1R,2R,3R)-3-Benzyloxy-2-((E)-(S)-3-benzyloxy-oct-1-enyl)-5-oxo-cyclopentyl]-hept-5-enoic acid 
• 145313-85-5 (Z)-7-[(1R,2R,3R,5S)-3-Benzyloxy-2-((E)-(S)-3-benzyloxy-oct-1-enyl)-5-hydroxy-cyclopentyl]-hept-5-enoic acid 
• 145313-83-3 (2R,3R,4R)-4-Benzyloxy-3-((E)-(S)-3-benzyloxy-oct-1-enyl)-2-((Z)-7-hydroxy-hept-2-enyl)-cyclopentanone 
• 137759-71-8 (3R,4R)-4-Benzyloxy-3-((E)-(S)-3-benzyloxy-oct-1-enyl)-2-methylene-cyclopentanone 
• 551-11-1 dinoprost 
• 145308-10-7 (3R,6S,7S)-3,7-Bis-benzyloxy-1,1-dimethoxy-dodec-4-yn-6-ol 
• 137821-04-6 (3R,6R,7S)-3,7-Bis-benzyloxy-1,1-dimethoxy-dodec-4-yn-6-ol 
• 137759-62-7 (3R,7S)-3,7-Bis-benzyloxy-1,1-dimethoxy-dodec-4-yn-6-ol 
• 137759-63-8 (3R,7S)-3,7-Bis-benzyloxy-1,1-dimethoxy-dodec-4-yn-6-one 
• 137759-67-2 C₃₀H₄₂O₄ 
• 137759-49-0 (4R,5R)-5-Benzyloxy-4-((E)-(S)-3-benzyloxy-oct-1-enyl)-3a,4,5,6-tetrahydro-3H-cyclopenta[c]isoxazole 
• 145414-87-5 (E)-(3R,6R,7S)-3,7-Bis-benzyloxy-1,1-dimethoxy-dodec-4-en-6-ol 
• 137759-69-4 (E)-(3R,4S,7S)-3,7-Bis-benzyloxy-4-vinyl-dodec-5-enal oxime 
• 137759-68-3 (E)-(3R,4S,7S)-3,7-Bis-benzyloxy-4-vinyl-dodec-5-enal 

Relevant academic research and scientific papers

New chiral synthetic intermediate for prostaglandins

Preparation of an optically active synthetic intermediate 3 starting from D-mannitol and its conversion to PGF2α (1) by using [3+2] cycloaddition of the nitrile oxide derivative of 3 followed by conjugate addition of the vinylzincate to exocyclic enone 2 are described.