Penazines 유도체를 합성하기 위하여 nitrosoaniline 의 중간단계를 거친 후 여러 극성용매에서 합성을 시도하 였고 BSA/DMF 시스템에서 고수율의 phenazined를 얻을 수 있었다.

Anions generated from primary arylamines react with substituted nitrobenzenes to form σH-adducts, which, under basic reaction conditions, undergo transformation to N-aryl-2-nitrosoamines. The substituted phenazines were furnished by the cyclization of N-aryl-2-nitrosoamines. The cyclization was promoted by N,O-bis(trimethylsilyl)acetamide (BSA) in aprotic solvents, by acetic acid and K2CO3/MeOH systems.

1. 서 론
 2. 실 험
  2.1. Materials and equipment
  2.2. General procedure for the preparationof substituted N-aryl-2-nitrosoanilines1
 3. 결과 및 고찰
 4. 결 론
 References

• 장진보(부경대학교 인쇄정보공학과) | Jinbo Zhang
• 손세모(부경대학교 인쇄정보공학과) | Semo Son 교신저자