Studies on enamides. Part-51: A novel pathway for photochemical reaction of N-1-cyclohexenyl-N-phenylarylamides

Tetrahedron Letters

Volumn 37, Issue 18, 1996, Pages 3169-3170

  Ghosh, Somnath ^a   Nandi, Bidisha ^a   Saima, Yasmin ^a  

^a JADAVPUR UNIVERSITY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ANILIDE; PHENANTHRIDINE DERIVATIVE;

ARTICLE; CYCLIZATION; DRUG SYNTHESIS; INFRARED SPECTROPHOTOMETRY; NUCLEAR MAGNETIC RESONANCE; PHOTOCHEMISTRY; REACTION ANALYSIS; STEREOCHEMISTRY; TECHNIQUE;

EID: 0029965307     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00242-0     Document Type: Article

References (7)

1. Part-4: Datta, I; Das, T.K. (in part); Ghosh, S.N. Tetrahedron 1990, 46, 6821.
2. Part-4: Datta, I; Das, T.K. (in part); Ghosh, S.N. Tetrahedron 1990, 46, 6821.
3. Reviews: a) Sharma, R.K.; Kharasch, N. Angew. Chem. Int. Ed. Engl. 1968, 7, 36;
4. b) Lenz, G.R. Synthesis, 1978, 489;
5. c) Mallory, F.B.; Mallory, C.W. Org. React. 1984, 30, 1.
6. Irradiation experiments were performed at room temperature using a low pressure mercury lamp (16 W, > 90% 254 nm, Applied Photophysics Ltd., England) in a quartz vessel (immersion type).
7. 2b on the nitrogen atom of enamides is known to afford rearranged products (1,3 - or 1,5 -) on non-oxidative photolysis.