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乙二醇
甲醛
63148-62-9
MDI
丁酮
二甲基亚砜
碳酸氢钠
471-34-1
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乙二醇
甲醛
63148-62-9
MDI
丁酮
二甲基亚砜
碳酸氢钠
471-34-1
Phomactin A
合成路线
(共 31 条)
501369-42-2
→
反应条件
130595-24-3
Phomactin A
反应条件
tetrabutyl ammonium fluoride in tetrahydrofuran T=0°C; 0.5 h;
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
89-82-7
长叶薄荷酮
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: 70 percent / LDA; LiCl 2.1: 75 percent / KOH / Heating 3.1: diisopropyl amine; n-butyllithium; triethylamine / chlorotrimethylsilane / tetrahydrofuran; petroleum ether / -78 - 0 °C 3.2: bromine / tetrahydrofuran; petroleum ether / 2 h / -78 °C 4.1: 5.0 g / lithium carbonate; lithium bromide / dimethylformamide / 4 h / 100 - 105 °C 5.1: diisopropyl amine; n-butyllithium / diethyl ether; petroleum ether / 0.58 h / -78 °C 5.2: diethyl ether; petroleum ether / 1 h / -78 °C 6.1: 378 mg / triethylamine; methanesulfonyl chloride / CH2Cl2 / 4 h / 20 °C 7.1: lithium chloride / tetrahydrofuran / 2 h / 20 °C 7.2: n-butyllithium / tetrahydrofuran; petroleum ether / 0.08 h / -78 °C 7.3: 70 percent / tetrahydrofuran; petroleum ether / 0.5 h / -78 °C 8.1: 91 percent / PCC / CH2Cl2 / 48 h / 20 °C 9.1: cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 10.1: 173 mg / mCPBA / CH2Cl2 / 1 h / 0 °C 11.1: 86 percent / Dess-Martin periodonane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 12.1: magnesium bromide diethyl etherate / CH2Cl2 / 12 h / -78 °C 13.1: 1.0 g / pyridine; trifluoroacetic anhydride; triethylamine / CH2Cl2 / 3.5 h / 0 - 20 °C 14.1: magnesium bromide diethyl etherate; butanethiol / diethyl ether / 15 h / 20 °C 14.2: 77 percent / camphorsulfonic acid / CH2Cl2 / 18 h / 20 °C 15.1: 94 percent / cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 16.1: triphenylphosphine; diethyl azodicarboxylate; 4-nitrobenzoic acid / tetrahydrofuran / 12 h / 20 °C 16.2: 86 percent / sodium methoxide / methanol / 1 h / 20 °C 17.1: 92 percent / imidazole / dimethylformamide / 2 h / 40 °C 18.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 18.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 19.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 20.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 21.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 22.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 23.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 24.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 25.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 25.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 26.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
234078-11-6
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: diisopropyl amine; n-butyllithium; triethylamine / chlorotrimethylsilane / tetrahydrofuran; petroleum ether / -78 - 0 °C 1.2: bromine / tetrahydrofuran; petroleum ether / 2 h / -78 °C 2.1: 5.0 g / lithium carbonate; lithium bromide / dimethylformamide / 4 h / 100 - 105 °C 3.1: diisopropyl amine; n-butyllithium / diethyl ether; petroleum ether / 0.58 h / -78 °C 3.2: diethyl ether; petroleum ether / 1 h / -78 °C 4.1: 378 mg / triethylamine; methanesulfonyl chloride / CH2Cl2 / 4 h / 20 °C 5.1: lithium chloride / tetrahydrofuran / 2 h / 20 °C 5.2: n-butyllithium / tetrahydrofuran; petroleum ether / 0.08 h / -78 °C 5.3: 70 percent / tetrahydrofuran; petroleum ether / 0.5 h / -78 °C 6.1: 91 percent / PCC / CH2Cl2 / 48 h / 20 °C 7.1: cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 8.1: 173 mg / mCPBA / CH2Cl2 / 1 h / 0 °C 9.1: 86 percent / Dess-Martin periodonane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 10.1: magnesium bromide diethyl etherate / CH2Cl2 / 12 h / -78 °C 11.1: 1.0 g / pyridine; trifluoroacetic anhydride; triethylamine / CH2Cl2 / 3.5 h / 0 - 20 °C 12.1: magnesium bromide diethyl etherate; butanethiol / diethyl ether / 15 h / 20 °C 12.2: 77 percent / camphorsulfonic acid / CH2Cl2 / 18 h / 20 °C 13.1: 94 percent / cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 14.1: triphenylphosphine; diethyl azodicarboxylate; 4-nitrobenzoic acid / tetrahydrofuran / 12 h / 20 °C 14.2: 86 percent / sodium methoxide / methanol / 1 h / 20 °C 15.1: 92 percent / imidazole / dimethylformamide / 2 h / 40 °C 16.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 16.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 17.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 18.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 19.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 20.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 21.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 22.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 23.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 23.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 24.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
501369-28-4
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: 75 percent / KOH / Heating 2.1: diisopropyl amine; n-butyllithium; triethylamine / chlorotrimethylsilane / tetrahydrofuran; petroleum ether / -78 - 0 °C 2.2: bromine / tetrahydrofuran; petroleum ether / 2 h / -78 °C 3.1: 5.0 g / lithium carbonate; lithium bromide / dimethylformamide / 4 h / 100 - 105 °C 4.1: diisopropyl amine; n-butyllithium / diethyl ether; petroleum ether / 0.58 h / -78 °C 4.2: diethyl ether; petroleum ether / 1 h / -78 °C 5.1: 378 mg / triethylamine; methanesulfonyl chloride / CH2Cl2 / 4 h / 20 °C 6.1: lithium chloride / tetrahydrofuran / 2 h / 20 °C 6.2: n-butyllithium / tetrahydrofuran; petroleum ether / 0.08 h / -78 °C 6.3: 70 percent / tetrahydrofuran; petroleum ether / 0.5 h / -78 °C 7.1: 91 percent / PCC / CH2Cl2 / 48 h / 20 °C 8.1: cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 9.1: 173 mg / mCPBA / CH2Cl2 / 1 h / 0 °C 10.1: 86 percent / Dess-Martin periodonane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 11.1: magnesium bromide diethyl etherate / CH2Cl2 / 12 h / -78 °C 12.1: 1.0 g / pyridine; trifluoroacetic anhydride; triethylamine / CH2Cl2 / 3.5 h / 0 - 20 °C 13.1: magnesium bromide diethyl etherate; butanethiol / diethyl ether / 15 h / 20 °C 13.2: 77 percent / camphorsulfonic acid / CH2Cl2 / 18 h / 20 °C 14.1: 94 percent / cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 15.1: triphenylphosphine; diethyl azodicarboxylate; 4-nitrobenzoic acid / tetrahydrofuran / 12 h / 20 °C 15.2: 86 percent / sodium methoxide / methanol / 1 h / 20 °C 16.1: 92 percent / imidazole / dimethylformamide / 2 h / 40 °C 17.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 17.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 18.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 19.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 20.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 21.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 22.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 23.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 24.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 24.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 25.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
501369-29-5
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: 5.0 g / lithium carbonate; lithium bromide / dimethylformamide / 4 h / 100 - 105 °C 2.1: diisopropyl amine; n-butyllithium / diethyl ether; petroleum ether / 0.58 h / -78 °C 2.2: diethyl ether; petroleum ether / 1 h / -78 °C 3.1: 378 mg / triethylamine; methanesulfonyl chloride / CH2Cl2 / 4 h / 20 °C 4.1: lithium chloride / tetrahydrofuran / 2 h / 20 °C 4.2: n-butyllithium / tetrahydrofuran; petroleum ether / 0.08 h / -78 °C 4.3: 70 percent / tetrahydrofuran; petroleum ether / 0.5 h / -78 °C 5.1: 91 percent / PCC / CH2Cl2 / 48 h / 20 °C 6.1: cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 7.1: 173 mg / mCPBA / CH2Cl2 / 1 h / 0 °C 8.1: 86 percent / Dess-Martin periodonane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 9.1: magnesium bromide diethyl etherate / CH2Cl2 / 12 h / -78 °C 10.1: 1.0 g / pyridine; trifluoroacetic anhydride; triethylamine / CH2Cl2 / 3.5 h / 0 - 20 °C 11.1: magnesium bromide diethyl etherate; butanethiol / diethyl ether / 15 h / 20 °C 11.2: 77 percent / camphorsulfonic acid / CH2Cl2 / 18 h / 20 °C 12.1: 94 percent / cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 13.1: triphenylphosphine; diethyl azodicarboxylate; 4-nitrobenzoic acid / tetrahydrofuran / 12 h / 20 °C 13.2: 86 percent / sodium methoxide / methanol / 1 h / 20 °C 14.1: 92 percent / imidazole / dimethylformamide / 2 h / 40 °C 15.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 15.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 16.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 17.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 18.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 19.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 20.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 21.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 22.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 22.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 23.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
501369-33-1
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: magnesium bromide diethyl etherate; butanethiol / diethyl ether / 15 h / 20 °C 1.2: 77 percent / camphorsulfonic acid / CH2Cl2 / 18 h / 20 °C 2.1: 94 percent / cerium trichloride; sodium borohydride / methanol / 0.5 h / 0 °C 3.1: triphenylphosphine; diethyl azodicarboxylate; 4-nitrobenzoic acid / tetrahydrofuran / 12 h / 20 °C 3.2: 86 percent / sodium methoxide / methanol / 1 h / 20 °C 4.1: 92 percent / imidazole / dimethylformamide / 2 h / 40 °C 5.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 5.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 6.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 7.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 8.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 9.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 10.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 11.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 12.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 12.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 13.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
501369-43-3
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: 82 percent / triethylamine; sulfur trioxide pyridine complex / CH2Cl2; dimethylsulfoxide / 1 h / 0 °C 2.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 2.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 3.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 4.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 5.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 6.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 7.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 8.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 9.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 9.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 10.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
102699-81-0
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: 10.5 g / imidazole / dimethylformamide / 12 h / 20 °C 2.1: bis(cyclopentadienyl)zirconium chloride hydride / benzene / 12 h / 40 °C 2.2: 65 percent / iodine / benzene / 0.08 h / 20 °C 3.1: 92 percent / TBAF / tetrahydrofuran / 0.5 h / 20 °C 4.1: isopropyl D-tartrate; titanium isopropoxide; tert-butylhydroperoxide / CH2Cl2 / 2 h / -20 °C 5.1: 82 percent / triethylamine; sulfur trioxide pyridine complex / CH2Cl2; dimethylsulfoxide / 1 h / 0 °C 6.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 6.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 7.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 8.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 9.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 10.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 11.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 12.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 13.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 13.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 14.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
139109-02-7
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: zinc; triphenylphosphine / CH2Cl2 / 1 h / 0 °C 1.2: CH2Cl2 / 5 h / 20 °C 2.1: n-butyllithium / diethyl ether; hexane / 1 h / 0 °C 3.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C 3.2: 816 mg / tetrahydrofuran; hexane / 3 h / 20 °C 4.1: TBAF / tetrahydrofuran / 1 h / 20 °C 5.1: 10.5 g / imidazole / dimethylformamide / 12 h / 20 °C 6.1: bis(cyclopentadienyl)zirconium chloride hydride / benzene / 12 h / 40 °C 6.2: 65 percent / iodine / benzene / 0.08 h / 20 °C 7.1: 92 percent / TBAF / tetrahydrofuran / 0.5 h / 20 °C 8.1: isopropyl D-tartrate; titanium isopropoxide; tert-butylhydroperoxide / CH2Cl2 / 2 h / -20 °C 9.1: 82 percent / triethylamine; sulfur trioxide pyridine complex / CH2Cl2; dimethylsulfoxide / 1 h / 0 °C 10.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 10.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 11.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 12.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 13.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 14.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 15.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 16.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 17.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 17.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 18.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
201849-60-7
→
反应条件
130595-24-3
Phomactin A
反应条件
1.1: bis(cyclopentadienyl)zirconium chloride hydride / benzene / 12 h / 40 °C 1.2: 65 percent / iodine / benzene / 0.08 h / 20 °C 2.1: 92 percent / TBAF / tetrahydrofuran / 0.5 h / 20 °C 3.1: isopropyl D-tartrate; titanium isopropoxide; tert-butylhydroperoxide / CH2Cl2 / 2 h / -20 °C 4.1: 82 percent / triethylamine; sulfur trioxide pyridine complex / CH2Cl2; dimethylsulfoxide / 1 h / 0 °C 5.1: t-butyllithium / diethyl ether; pentane / 0.5 h / -78 °C 5.2: 51 percent / TMEDA / diethyl ether; pentane / 0.08 h / -78 °C 6.1: 90 percent / Dess-Martin periodinane; sodium bicarbonate / CH2Cl2 / 1 h / 20 °C 7.1: TBAF / tetrahydrofuran / 0.5 h / 0 °C 8.1: 25 mg / HCl / 2-methyl-butan-2-ol / 2 h / 20 °C 9.1: 83 percent / imidazole / dimethylformamide / 2 h / 20 °C 10.1: 87 percent / DDQ / CH2Cl2; H2O / 0.5 h / 20 °C 11.1: 81 percent / pyridine / CH2Cl2 / 0.17 h / -78 °C 12.1: 9-BBN / tetrahydrofuran / 2 h / 40 °C 12.2: 37 percent / thallium carbonate; triphenylarsine / [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) / tetrahydrofuran; dimethylformamide; H2O / 12 h / 20 °C 13.1: 78 percent / TBAF / tetrahydrofuran / 0.5 h / 0 °C View Scheme
参考文献
Mohr, Peter J.; Halcomb, Randall L.
Journal of the American Chemical Society, 2003 , vol. 125, # 7 p. 1712 - 1713
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