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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
121587-29-9
合成路线
（共 7 条）
121587-29-9
→
反应条件
308357-81-5
4-[(1E,3S,5Z,8R/S,10S)-3,11-二-{[叔-丁基(二甲基)硅烷基]氧基}-2,6,10-三甲基-8-(苯磺酰基)十一碳-1,5-二烯基]-2-甲基-1,3-噻唑
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
121587-29-9
→
反应条件
193146-53-1
(3S,6R,7S,8S,12Z,15S,16E)-3,7,15-三-{[叔-丁基(二甲基)硅烷基]氧基}-1-羟基-4,4,6,8,12,16-六甲基-17-(2-甲基-1,3-噻唑-4-基)十七-12,16-二烯-5-酮
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C 3.1: 65 percent / Na2HPO4; Na-Hg amalgam / methanol; tetrahydrofuran / -15 - 20 °C 4.1: 99 percent / CSA / methanol; CH2Cl2 / 5 h / 0 - 10 °C 5.1: Dess-Martin periodinane; pyridine / CH2Cl2 / 4 h / 20 °C 6.1: LDA / tetrahydrofuran / 1 h / -78 - -35 °C 6.2: tetrahydrofuran / 1.5 h / -95 - -80 °C 7.1: 99 percent / 2,6-lutidine / CH2Cl2 / 3 h / 0 °C 8.1: 87 percent / CSA / methanol; CH2Cl2 / 4 h / 0 °C View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
121587-29-9
→
反应条件
152044-54-7
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C 3.1: 65 percent / Na2HPO4; Na-Hg amalgam / methanol; tetrahydrofuran / -15 - 20 °C 4.1: 99 percent / CSA / methanol; CH2Cl2 / 5 h / 0 - 10 °C 5.1: Dess-Martin periodinane; pyridine / CH2Cl2 / 4 h / 20 °C 6.1: LDA / tetrahydrofuran / 1 h / -78 - -35 °C 6.2: tetrahydrofuran / 1.5 h / -95 - -80 °C 7.1: 99 percent / 2,6-lutidine / CH2Cl2 / 3 h / 0 °C 8.1: 87 percent / CSA / methanol; CH2Cl2 / 4 h / 0 °C 9.1: Dess-Martin periodinane; Py / CH2Cl2 / 2 h / 20 °C 10.1: 380 mg / NaClO2; NaH2PO4 / 2-methyl-propan-2-ol; various solvent(s); H2O / 3 h 11.1: 55 percent / TBAF / tetrahydrofuran / 10 h / 20 °C 12.1: 69 percent / N-ethyl-N'-(3-(dimethylamino)propyl)carbodiimide *HCl; DMAP; DMAP*HCl / CHCl3 / 17 h / Heating 13.1: 96 percent / HF*Py; Py / tetrahydrofuran / 36 h / 0 - 20 °C 14.1: m-CPBA / CHCl3 / 5 h / -18 °C View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
121587-29-9
→
反应条件
189453-10-9
Epothilone D
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C 3.1: 65 percent / Na2HPO4; Na-Hg amalgam / methanol; tetrahydrofuran / -15 - 20 °C 4.1: 99 percent / CSA / methanol; CH2Cl2 / 5 h / 0 - 10 °C 5.1: Dess-Martin periodinane; pyridine / CH2Cl2 / 4 h / 20 °C 6.1: LDA / tetrahydrofuran / 1 h / -78 - -35 °C 6.2: tetrahydrofuran / 1.5 h / -95 - -80 °C 7.1: 99 percent / 2,6-lutidine / CH2Cl2 / 3 h / 0 °C 8.1: 87 percent / CSA / methanol; CH2Cl2 / 4 h / 0 °C 9.1: Dess-Martin periodinane; Py / CH2Cl2 / 2 h / 20 °C 10.1: 380 mg / NaClO2; NaH2PO4 / 2-methyl-propan-2-ol; various solvent(s); H2O / 3 h 11.1: 55 percent / TBAF / tetrahydrofuran / 10 h / 20 °C 12.1: 69 percent / N-ethyl-N'-(3-(dimethylamino)propyl)carbodiimide *HCl; DMAP; DMAP*HCl / CHCl3 / 17 h / Heating 13.1: 96 percent / HF*Py; Py / tetrahydrofuran / 36 h / 0 - 20 °C View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
121587-29-9
→
反应条件
193146-51-9
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C 3.1: 65 percent / Na2HPO4; Na-Hg amalgam / methanol; tetrahydrofuran / -15 - 20 °C 4.1: 99 percent / CSA / methanol; CH2Cl2 / 5 h / 0 - 10 °C 5.1: Dess-Martin periodinane; pyridine / CH2Cl2 / 4 h / 20 °C 6.1: LDA / tetrahydrofuran / 1 h / -78 - -35 °C 6.2: tetrahydrofuran / 1.5 h / -95 - -80 °C 7.1: 99 percent / 2,6-lutidine / CH2Cl2 / 3 h / 0 °C View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
121587-29-9
→
反应条件
193146-63-3
(3S,6R,7S,8S,12Z,15S,16E)-3,7,15-三-{[叔-丁基(二甲基)硅烷基]氧基}-4,4,6,8,12,16-六甲基-17-(2-甲基-1,3-噻唑-4-基)-5-氧代-十七-12,16-二烯酸
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C 3.1: 65 percent / Na2HPO4; Na-Hg amalgam / methanol; tetrahydrofuran / -15 - 20 °C 4.1: 99 percent / CSA / methanol; CH2Cl2 / 5 h / 0 - 10 °C 5.1: Dess-Martin periodinane; pyridine / CH2Cl2 / 4 h / 20 °C 6.1: LDA / tetrahydrofuran / 1 h / -78 - -35 °C 6.2: tetrahydrofuran / 1.5 h / -95 - -80 °C 7.1: 99 percent / 2,6-lutidine / CH2Cl2 / 3 h / 0 °C 8.1: 87 percent / CSA / methanol; CH2Cl2 / 4 h / 0 °C 9.1: Dess-Martin periodinane; Py / CH2Cl2 / 2 h / 20 °C 10.1: 380 mg / NaClO2; NaH2PO4 / 2-methyl-propan-2-ol; various solvent(s); H2O / 3 h View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
121587-29-9
→
反应条件
193146-49-5
(3S,6R,7S,8S,12Z,15S,16E)-1,3,15-三-{[叔-丁基(二甲基)硅烷基]氧基}-7-羟基-4,4,6,8,12,16-六甲基-17-(2-甲基-1,3-噻唑-4-基)十七烷基-12,16-二烯-5-酮
反应条件
1.1: 99 percent / imidazole / dimethylformamide / 3 h / 0 - 20 °C 2.1: 18-crown-6; KHMDS / tetrahydrofuran / 1 h / -78 °C 2.2: 93 percent / tetrahydrofuran / 1 h / -78 °C 3.1: 65 percent / Na2HPO4; Na-Hg amalgam / methanol; tetrahydrofuran / -15 - 20 °C 4.1: 99 percent / CSA / methanol; CH2Cl2 / 5 h / 0 - 10 °C 5.1: Dess-Martin periodinane; pyridine / CH2Cl2 / 4 h / 20 °C 6.1: LDA / tetrahydrofuran / 1 h / -78 - -35 °C 6.2: tetrahydrofuran / 1.5 h / -95 - -80 °C View Scheme
参考文献
Mulzer, Johann; Mantoulidis, Andreas; Oehler, Elisabeth
Journal of Organic Chemistry, 2000 , vol. 65, # 22 p. 7456 - 7467
