Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Patent
1995-05-04
1997-08-05
Berch, Mark L.
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C07D20508, C07D40504, C07F 710
Patent
active
056544243
ABSTRACT:
The present invention is directed to a process of making a Beta-methyl carbapenem intermediate of formula VI from a compound of formula I ##STR1## wherein R and P' are protecting groups R.sup.1 is a methylmalonic acid ester and Nu is a nucleophilic group. Process intermediates are also disclosed.
REFERENCES:
patent: 4576746 (1986-03-01), Favara et al.
patent: 4801719 (1989-01-01), Oertle et al.
patent: 4960880 (1990-10-01), Uyeo
patent: 4992545 (1991-02-01), Hall et al.
patent: 5371214 (1994-12-01), Miura
Tetrahedron Letters, vol. 26, No. 39, pp. 4739-4742 (1985), by T. Shibata, et al.
J. Am. Chem. Soc. 1986, 108, 4673-4675, by Y. Nagao, et al.
Tetrahedron Letters, vol. 27, No. 19, pp. 2149-2152, 1986, by T. Iimori, et al.
Tetrahedron Letters, vol. 27, No. 51, pp. 6241-6244, 1986, by T. Kawabata, et al.
Can. J. Chem., vol. 65, 1987, pp. 2140-2145, by M. Endo.
J. Org. Chem, 1987, vol. 52, pp. 3174-3176, by R. Funk, et al.
J. Org. Chem. 1987, vol. 52, pp. 2563-2567 by L. Fuentes, et al.
Tetrahedron Letters, vol. 28, No. 1, pp. 83-86, 1987, by M. Hatanaka.
Tetrahedron Letters, vol. 28, No. 5, pp. 507-510, 1987, by C. Kim, et al.
Tetrahedron Letters, vol. 28, No. 17, pp. 1857-1860, 1987, by J. Prasad, et al.
Tetrahedron Letters, vol. 28, No. 52, pp. 6625-6628, 1987, by Y. Ito, et al.
Can. J. Chem., vol. 66, pp. 1400-1404, 1987, by M. Endo, et al.
Can. J. Chem. vol. 66, 1988, pp. 1537-1539, by A. Martel, et al.
J. Org. Chem. 1988, vol. 53, pp. 212902131, by Ni, et al.
J. Org. Chem. 1988, vol. 53, pp. 4154-4156, by Sowin et al.
Tetrahedron, vol. 44, No. 8, pp. 2149-2156, by T. Kawabata, et al. (1988).
Tetrahedron Letters, vol. 29, No. 1, pp. 61-64, 1988, by R. Deziel, et al.
Tetrahedron Letters, vol. 29, No. 48, pp. 6345-6348, by R. Bayles, et al. (1988).
Chem. Letters, 1989, pp. 445-448, by F. Shirai, et al.
J. Org. Chem. 1989, vol. 54, pp. 2103-2112, by U. Udodong, et al.
Tetrahedron Letters, vol. 30, No. 1, pp. 113-116, 1989, by H. Kaga, et al.
Tetrahedron Letters, vol. 31, No. 2, pp. 271-274, 1990, by A. Rao, et al.
Tetrahedron Letters, vol. 31, No. 4, pp. 549-552, 1990, by M. Kitamura, et al.
Chem. Pharm. Bull, vol. 39, No. 9, pp. 2225-2232, 1991, by Y. Kita, et al.
Tetrahedron, vol. 47, No. 16/17, pp. 2801-2820, 1991, by Y. Ito, et al.
Tetrahedron: Asymmetry, vol. 2, No. 4, pp. 255-256, 1991, by A. Rao, et al.
Tetrahedron Letters, vol. 32, No. 19, pp. 2143-2144, 1991, by S. Uyeo, et al.
J. Org. Chem. 1992, vol. 57, pp. 2411-2418, by D. Bender, et al.
Tetrahedron, vol. 48, No. 1, pp. 55-66, 1992, by Y. Kobayashi, et al.
Tetrahedron Letters, vol. 29, No. 49, pp. 6461-6464, 1988, by F. Shirai, et al.
Tetrahedron Letters, vol. 32, pp. 2471-2474, 1991, by D. Barton, et al.
J.A.C.S., vol. 76, pp. 5563-5564, 1954, by C. Hurd, et al.
Organic Syntheses Collective, vol. 3, pp. 212-216, by J. Callen, et al. (1950).
Synlett, pp. 407-409, Jun. 1991, by A. Arcadi, et al.
Indian J. of Chem., vol. 16B, Jun. 1978, pp. 449-451, by O. Vig, et al.
Indian J. of Chem., vol. 16B, Feb. 1978, pp. 114-115, by O. Vig, et al.
Heterocycles, vol. 17, 1982, pp. 463-506, by T. Kametani.
Heterocycles, vol. 35, No. 1, pp. 139-142, 1993, by Ihara, et al.
Chemistry Letters, No. 4, 1990, pp. 531-534, by T. Honda, et al.
Heterocycles, vol. 19, No. 6, 1982, pp. 1023-1032, by T. Kametani, et al.
Choi Woo-Baeg
Humphrey Guy R.
Reider Paul J.
Shinkai Ichiro
Thompson Andrew S.
Berch Mark L.
Billups Richard C.
Daniel Mark R.
Merck & Co. , Inc.
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