Stereoselective solid-phase synthesis of 3,4-substituted azetidinones as key intermediates for mono- and multicyclic β-lactam antibiotics and enzyme inhibitors-Reference-Cited by-同舟云学术

Stereoselective solid-phase synthesis of 3,4-substituted azetidinones as key intermediates for mono- and multicyclic β-lactam antibiotics and enzyme inhibitors

Published:2002-06 Issue:9 Volume:13 Page:905-910
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Delpiccolo Carina M.L.,Mata Ernesto G.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference32 articles.

1. The Organic Chemistry of β-Lactams, Georg, G. I., Ed; VCH: New York, 1993.

2. Bose, A. K.; Banik, B. K.; Mathur, C.; Wagle, D. R.; Manhas, M. S. Tetrahedron 2000 56, 5603–5619.

3. Rosenblum, S. B.; Huynh, T.; Afonso, A.; Davis, H. R.; Yumibe, N.; Clader, J. W.; Burnett, D. A. J. Med. Chem. 1998, 41, 973–980 and references cited therein.

4. Zaragoza Dörwald, F. Organic Synthesis on Solid Phase; Wiley-VCH, Weinheim, 2000

5. Solid-Phase Organic Synthesis, Burgess, K., Ed.; Wiley-Interscience, New York, 2000.

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