One-step synthesis of substituted 4,8-dihydropyrano[3,2-b]pyran-4-ones [3]

Russian Chemical Bulletin

Volumn 53, Issue 3, 2004, Pages 724-725

  Shestopalov, A A ^a   Rodinovskaya, L A ^a   Shestopalov, A M ^a   Litvinov, V P ^a  

^a N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

4 PYRONE DERIVATIVE;

CALCULATION; CROSS REACTION; CRYSTALLIZATION; LETTER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRECIPITATION; SUBSTITUTION REACTION; SYNTHESIS;

EID: 4043084182     PISSN: 10665285     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:RUCB.0000035666.05686.89     Document Type: Letter

References (6)

1. The Merck Index, Eds V. J. O'Neil, Merck and Co., Inc., Whitehouse Station, NJ, 2001, 951 p.
2. M.-Z. Piao and K. Imafuku, Tetrahedron Lett., 1997, 38, 5301.
3. S. Wang, G. W. A. Milne, X. Yang, I. J. Posey, M. C. Nicklaus, L. Graham, and W. G. Rice, J. Med. Chem., 1996, 39, 2047.
4. V. P. Litvinov and A. M. Shestopalov, Zh. Org. Khim., 1997, 33, 975 [Russ. J. Org. Chem., 1997, 33, 926 (Engl. Transl.)].
5. V. P. Litvinov and A. M. Shestopalov, Zh. Org. Khim., 1997, 33, 975 [Russ. J. Org. Chem., 1997, 33, 926 (Engl. Transl.)].
6. A. M. Shestopalov, Y. M. Emeliyanova, A. A. Shestopalov, L. A. Rodinovskaya, Z. I. Niazimbetova, and D. H. Evans, Tetrahedron, 2003, 59, 7491.