Baeyer–Emmerling indole synthesis

Baeyer–Emmerling indole synthesis jẹ́ ọ̀nà fún ìṣètò indole lati (ìrọ́pò) ortho-nitrocinnamic acid àti iron gbẹrẹfu nínú àpòpọ̀ base tó le.[1][2] Ẹni tí ó ṣe àwàrí ìdàpapọ̀ ṣiṣẹ́ yìí ni Adolf von Baeyer àti Adolph Emmerling ní ọdún 1869.[3] [4]

Baeyer-Emmerling indole synthesis
Baeyer-Emmerling indole synthesis

Ètò ìdàpọ̀ ṣiṣẹ́

àtúnṣe

Ìdàpọ̀ ṣiṣẹ́ iron gbẹrẹfu pẹ̀lú  o-nitrocinnamic mú ẹgbẹ́ nito kù sí nitroso. Nitrogen yìí maa dìpọ̀ pẹ̀lú carbon lórí okùn alkene pẹ̀lú sísọ molecule omi kan nù lati di ohun róbótó. Yíyọ ẹgbẹ́ carbonyl kúro ma a jẹ́ kí indole jẹyọ.

 
Baeyer-Emmerling indole reaction mechanism

Àwọn ìtọ́kasí

àtúnṣe
  1. Bayer, A.; Emmerling, A. (1869). "Synthese des indoles". Berichte der deutschen chemischen Gesellschaft 2 (1): 679–682. doi:10.1002/cber.186900201268. 
  2. Baeyer 5 Archived 2007-08-16 at the Wayback Machine..
  3. Chamberlain, Joseph Scudder (1921). A Textbook of Organic Chemistry. Blakiston. p. 874. http://books.google.com/books?id=9ls6AAAAMAAJ&pg=PA874. 
  4. Lockyer, Sir Norman (1881). "Indigo and its Artificial Production". Nature 24 (610): 227. doi:10.1038/024227c0. http://books.google.com/books?id=TMMKAAAAYAAJ&pg=PA229.