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Volumn 30, Issue 42, 1989, Pages 5703-5704

Intramolecular photocycloaddition and retro-mannich fragmentation of acyclic tertiary vinylogous amides

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0040979441 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)76175-2 Document Type: Article

Times cited : (14)

References (8)

1
- 0023690543
- (1988) J. Am. Chem. Soc. , vol.110 , pp. 4831
- Winkler¹ Muller² Scott³

2
- 0000225034
- For the photochemical synthesis of 2-azabicyclo[2.1.1]hexane ring systems via the intramolecular photocycloaddition of vinylogous amides, see
- (1975) J. Org. Chem. , vol.40 , pp. 2702
- Tamura¹ Ishibashi² Hirai³ Kita⁴ Ikeda⁵

3
- 0000544915
- For the photocycloaddition of vinylogous imides, see, and references cited therein
- (1987) Tetrahedron Lett. , pp. 5275
- Swindell¹ Patel²

4
- 0006499663
- For an earlier example of the photocycloaddition/retro-Mannich fragmentation of a secondary vinylogous amide to give a ketoimine (without the final Mannich ring closure), see
- (1984) J. Org. Chem. , vol.49 , pp. 4067
- Schell¹ Cook²

5
- 33845278846
- and references cited therein
- (1988) Chemical Reviews , vol.88 , pp. 1453
- Crimmins¹

6
- 84918627154
- All new compounds were characterized by full spectroscopic data. Yields refer to spectroscopically and chromatographically homogeneous (〉95%) materials.

8
- 84918610906
- Support from the Petroleum Research Fund, administered by the American Chemical Society, the National Institutes of Health (CA 40250 and 45686), the Alfred P. Sloan Foundation, American Cyanamid, Merck, Sharp and Dohme, and Glaxo is gratefully acknowledged. The NMR instruments used were funded in part by the NSF Chemical Instrumentation Program and by the NCI via the University of Chicago Cancer Research Center (CA 14599).

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