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ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester

Base Information
  • Chemical Name:ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester
  • CAS No.:75884-81-0
  • Molecular Formula:C20H24O5
  • Molecular Weight:344.408
  • Hs Code.:
ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester

Synonyms:

Suppliers and Price of ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester
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Chemical Property of ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester
Chemical Property:
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Technology Process of ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester

There total 11 articles about ent-3β,10β-dihydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 19,10β-lactone 7-methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium tetrahydroborate; lithium bromide; In tetrahydrofuran; at 0 ℃; for 1h; Product distribution; Mechanism; other solvents (diglyme, pyridine); reduction with NaBH4-LiBr; H2O-HCl and D2O-DCl work-up; location and stereochemistry of deuterium incorporation;
Guidance literature:
Multi-step reaction with 3 steps
1: 310 mg / pyridine / Ambient temperature
2: 160 mg / potassium acetate / acetone; H2O / 5 h / Heating
3: 120 mg / tri-n-butyltin hydride, azobisisobutyronitrile / benzene / 1 h / Heating
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; potassium acetate; In pyridine; water; acetone; benzene;
Guidance literature:
Multi-step reaction with 4 steps
1: 160 mg / potassium acetate / acetone; H2O / 3.5 h / Heating
2: 310 mg / pyridine / Ambient temperature
3: 160 mg / potassium acetate / acetone; H2O / 5 h / Heating
4: 120 mg / tri-n-butyltin hydride, azobisisobutyronitrile / benzene / 1 h / Heating
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; potassium acetate; In pyridine; water; acetone; benzene;
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