Новые возможности внутримолекулярной реакции Ульмана в синтезе гетероциклических соединений
Диссертация
Исторически кислоту 1 получали в результате декарбоксилирования бензофуран-2,3-дикарбоновой кислоты или литиированием с последующим карбоксилированием 3-бромобензофурана. Оба этих метода не отличаются высокими выходами целевого соединения из-за побочных процессов. В первом случае в значительном количестве образуется незамещенный бензофуран — продукт двойного декарбоксилирования, во втором… Читать ещё >
Содержание
- 1. Введение
- 2. Внутримолекулярные реакции кросс-сочетания, катализируемые солями меди: 7 Эффективный инструмент синтеза гетероциклических соединений обзор литературы)
- 2. 1. Введение
- 2. 2. Общее рассмотрение механизма реакции Ульмана
- 2. 3. Реакции образования связи С-О
- 2. 3. 1. Четырехчленные гетероциклические соединения 15 2.3.1.1. Оксетаны
- 2. 3. 2. Пятичленные гетероциклические соединения
- 2. 3. 2. 1. Фураны и бензофураны
- 2. 3. 2. 2. Бензоксазолы
- 2. 3. 3. Шестичленные гетероциклические соединения
- 2. 3. 3. 1. Пираны и бензопираны
- 2. 3. 3. 2. Бензоксазины
- 2. 3. 3. 3. Дибензотиазины
- 2. 3. 3. 4. Бензодиоксаны
- 2. 3. 4. Семичленные гетероциклические соединения 37 2.3.4. Макрогетероциклические соединения
- 2. 4. Реакции образования связи C-S
- 2. 4. 1. Четырехчленные гетероциклические соединения 43 2.4.1.1. Тиетаны
- 2. 4. 2. Пятичленные гетероциклические соединения
- 2. 4. 2. 1. Тетрагидротиофены
- 2. 4. 2. 2. 1,3-Бензоксатиолы
- 2. 4. 2. 3. 1,3-Бензотиазолы
- 2. 4. 3. Шестичленные гетероциклические соединения 49 2.4.3.1. Тиопираны
- 2. 5. Реакции образования связи C-N
- 2. 5. 1. Четырехчленные гетероциклические соединения 49 2.5.1.1. Азетидины
- 2. 5. 2. Пятичленные гетероциклические соединения
- 2. 5. 2. 1. Пирролы и индолы
- 2. 5. 2. 2. Бензимидазолы 75 2.5.2.3 Индазолы 11 2.5.3 Шестичленные гетероциклические соединения
- 2. 5. 3. 1. Пиридины
- 2. 5. 3. 2. Хинролины
- 2. 5. 3. 3. Хиназолины
- 2. 5. 3. 4. 1,2,4-Бензотиадиазины
- 2. 5. 4. Семичленные гетероциклические соединения 89 2.5.4.1. Азепины и оксазепины
- 2. 5. 5. Восьмичленные гетероциклические соединения
- 2. 5. 6. Макрогетероциклические соединения 92
- 3. 1. Синтез эфиров бензофуран-3-карбоновых кислот
- 3. 2. Синтез производных Ш-индол-З-карбоновых кислот
- 3. 3. Простой синтез метилового эфира 1-(1,1 -диметилпроп-2-ен-1-ил)-17/- 118 индол-3-карбоновой кислоты
- 3. 4. Синтез метиловых эфиров 1-амино-1//-индол-3-карбоновых кислот 122 3.5 Синтез метиловых эфиров 1-алкокси-1Л-индол-3-карбоновых кислот 130 3.6. Синтез шестичленных гетероциклических соединений
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