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N-Boc dihydroanatoxin-a

Base Information
  • Chemical Name:N-Boc dihydroanatoxin-a
  • CAS No.:96997-82-9
  • Molecular Formula:C15H25NO3
  • Molecular Weight:267.368
  • Hs Code.:
N-Boc dihydroanatoxin-a

Synonyms:

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Chemical Property of N-Boc dihydroanatoxin-a
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Technology Process of N-Boc dihydroanatoxin-a

There total 25 articles about N-Boc dihydroanatoxin-a 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 chloro-trimethyl-silane; sodium iodide; In acetonitrile; for 0.0833333h; Ambient temperature;
Guidance literature:
Multi-step reaction with 14 steps
1: CH2Cl2
2: 88 percent / AgBF4 / CH2Cl2 / 72 h / Ambient temperature
3: CF3CO2H / CH2Cl2 / Ambient temperature
4: pyridine / 0 °C
5: 1) B2H6, 2) aq. NaOH, 30percent aq. H2O2 / 1) THF, 20 deg C, 20 min, 2) 30 min, room temp.
6: 63 percent / tetrahydrofuran / 0.17 h / -10 °C
7: 78 percent / PPh3, 2 M Br2 / tetrahydrofuran / a) 0 deg C, 10 min, b) up to room temp.
8: 83 percent / NaH / dimethylsulfoxide / 2 h / 40 °C
9: 92 percent / Al-Hg / tetrahydrofuran; H2O / 3 h / 60 °C
10: 1) LDA / 1) DME, hexane, -78 deg C, 20 min, 2) DME, 5 min
11: NaH / tetrahydrofuran / 14 h / Ambient temperature
12: liquid ammonia, lithium / tetrahydrofuran / 0.05 h / -78 °C
13: methanol / 16 h
14: 65 percent / (CH3)3SiCl, NaI / acetonitrile / 0.08 h / Ambient temperature
With pyridine; sodium hydroxide; chloro-trimethyl-silane; aluminium amalgam; ammonia; dihydrogen peroxide; bromine; lithium; sodium hydride; triphenylphosphine; trifluoroacetic acid; sodium iodide; diborane; lithium diisopropyl amide; silver tetrafluoroborate; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;
Guidance literature:
Multi-step reaction with 15 steps
1: 59 percent / aq. HCl / diethyl ether / 0.67 h / Ambient temperature
2: CH2Cl2
3: 88 percent / AgBF4 / CH2Cl2 / 72 h / Ambient temperature
4: CF3CO2H / CH2Cl2 / Ambient temperature
5: pyridine / 0 °C
6: 1) B2H6, 2) aq. NaOH, 30percent aq. H2O2 / 1) THF, 20 deg C, 20 min, 2) 30 min, room temp.
7: 63 percent / tetrahydrofuran / 0.17 h / -10 °C
8: 78 percent / PPh3, 2 M Br2 / tetrahydrofuran / a) 0 deg C, 10 min, b) up to room temp.
9: 83 percent / NaH / dimethylsulfoxide / 2 h / 40 °C
10: 92 percent / Al-Hg / tetrahydrofuran; H2O / 3 h / 60 °C
11: 1) LDA / 1) DME, hexane, -78 deg C, 20 min, 2) DME, 5 min
12: NaH / tetrahydrofuran / 14 h / Ambient temperature
13: liquid ammonia, lithium / tetrahydrofuran / 0.05 h / -78 °C
14: methanol / 16 h
15: 65 percent / (CH3)3SiCl, NaI / acetonitrile / 0.08 h / Ambient temperature
With pyridine; hydrogenchloride; sodium hydroxide; chloro-trimethyl-silane; aluminium amalgam; ammonia; dihydrogen peroxide; bromine; lithium; sodium hydride; triphenylphosphine; trifluoroacetic acid; sodium iodide; diborane; lithium diisopropyl amide; silver tetrafluoroborate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; dimethyl sulfoxide; acetonitrile;
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