TY - JOUR ID - 131552 TI - A Short Synthesis of Carbazole Alkaloids Murrayanine and Mukonine JO - Chemical Methodologies JA - CHEMM LA - en SN - 2645-7776 AU - Gaikwad, Milind V. AU - Kamble, Rahul D. AU - Hese, Shrikant V. AU - Kadam, Shuddhodan N. AU - Abhore, Ajay N. AU - Gaikwad, Sunil V. AU - Acharya, Ashok P. AU - Dawane, Bhaskar S. AD - Department of Chemistry, D.Y. Patil ACS College Pimpri, affiliated; Savitribai Phule Pune University, Pune (MS) India-411018 AD - Department of Chemistry, Amruteshwar ACS, College, Vinzar, Pune (MS) India-412213 AD - D.D. Bhoyar College of Arts and Science Mouda, Nagpur, 441104, MS, India AD - Department of Chemistry, VidnyanMahavidhyalaya, Sangola, Solapur (MS) India -413307 AD - Department of Chemistry, PDVP College, Tasgaon, Sangli (MS) India -416312 AD - Department of Chemistry, Savitribai Phule Pune University, Pune (MS) India-411007 AD - Department of chemistry Mudhoji College, Phaltan- Satara(MS) India-415523 AD - School of Chemical Sciences, SRTM University, Nanded (MS) India -431606 Y1 - 2021 PY - 2021 VL - 5 IS - 4 SP - 341 EP - 347 KW - Carbazole Alkaloids KW - Mukonine KW - Murrayanine KW - Buchard coupling DO - 10.22034/chemm.2021.131552 N2 - The short, easy and total synthesis of Murrayanine (1),  Mukonine (2), carbazole alkaloids were elaborated, based on a regioselective buchwald coupling of methyl 4-bromo-3-methoxybenzoate  with aniline and successive transformation into the corrsponding carbazole alkaloids by  oxidative coupling followed by cyclization of the phenyl and aryl rings.   UR - https://www.chemmethod.com/article_131552.html L1 - https://www.chemmethod.com/article_131552_8468c1a71b52d48db4f9e7bcdf4783e8.pdf ER -