Тёмный

The Buchwald-Hartwig Amination Reaction 

chemtubeuk
Подписаться 7 тыс.
Просмотров 11 тыс.
50% 1

Опубликовано:

 

23 сен 2024

Поделиться:

Ссылка:

Скачать:

Готовим ссылку...

Добавить в:

Мой плейлист
Посмотреть позже
Комментарии : 7   
@melekhthechanger88
@melekhthechanger88 7 лет назад
Hi thanks for that video! Massive long shot I know but having real problems with this coupling reaction using a primary aryl amine and aryl bromide. Any tips for what kind of phosphines I might be able to use to help this? Or useful papers? Thanks in advance.
@JamBear
@JamBear 7 лет назад
Hans Eckhardt look up a review by Surry and Buchwald called "binary phosphine ligands: a users guide" (or something like that).
@BlakeMichealPatton
@BlakeMichealPatton 3 года назад
excellent video
@botondbolgar7449
@botondbolgar7449 2 года назад
You have a mistake in the reductive elimination step. You have a C (the one on which is the H which migrates) next to the N, which comes from nowhere.
@chemtubeuk
@chemtubeuk 2 года назад
Hi Botond, I relabelled the R1 group to R1' in the video when I discussed the beta hydride by-product (note the prime to show it is a derivative of R1). Does that help? I admit the prime is difficult to spot in the video if the resolution is low on playback.
@tahani91kh80
@tahani91kh80 5 лет назад
I have a question please
@Chem_hub.official
@Chem_hub.official 4 года назад
What??
Далее
Unique deep painful back massage for Lisa #chiropractor
00:11
Suzuki Coupling   Mechanism and Applications
12:15
Просмотров 58 тыс.
Sonogashira Coupling - A Practical Approach
33:58
Просмотров 12 тыс.
ORGANIC CHEMISTRY explained in 8 Minutes
8:39
Просмотров 1,4 тыс.
Buchwald-Hartwig Reaction
6:12
Просмотров 9 тыс.
BUCHWALD-HARTWIG REACTION
10:01
Просмотров 32
Buchwald-Hartwig cross-coupling reaction
3:49
Просмотров 4,1 тыс.