Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Polymers from only ethylenic monomers or processes of...
Patent
1992-07-31
1994-01-18
Nutter, Nathan M.
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Polymers from only ethylenic monomers or processes of...
526348, 5263482, 5263483, 5263486, C08F 1202, C08F11202
Patent
active
052800962
ABSTRACT:
Optically active polymers are of the formula ##STR1## wherein R and R.sup.1 are different from each other and are selected from the group consisting of (C.sub.1 -C.sub.20)alkyl, (C.sub.2 -C.sub.20)alkenyl, (C.sub.2 -C.sub.20)alkynyl, (C.sub.3 -C.sub.22) cycloalkyl and (C.sub.6 -C.sub.22)aryl, the alkyl, alkenyl and alkynyl further including an atom selected from the group consisting of N, O and S in the chain, the alkyl, alkenyl and alkynyl further including a substituent selected from the group consisting of (C.sub.1 -C.sub.4)alkyl and halogen atoms, the cycloalkyl and aryl further including an atom selected from the group consisting of N, O and S in the ring, and the cycloalkyl and aryl further including a substituent selected from the group consisting of (C.sub.1 -C.sub.10)alkoxy, aryloxy, halogen atoms, NO.sub.2 and NHCOR.sup.4 wherein R.sup.4 is selected from the group consisting of (C.sub.1 -C.sub.6)alkyl, (C.sub.2 -C.sub.6)alkenyl, (C.sub.2 -C.sub.6)alkynyl and (C.sub.6 -C.sub.10)aryl; R.sup.2 is selected from the group consisting of --CO--, --CO--R.sup.3 --CO--, (CH.sub.2).sub.q, --C.sub.6 H.sub.4 --, 4,4'-biphenylene and --OCNH--R.sup.3 --NHCO-- wherein R.sup.3 is selected from the group consisting of (C.sub.1 -C.sub.10)alkyl, (C.sub.2 -C.sub.10)alkenyl, (C.sub.2 -C.sub.10)alkynyl, (C.sub.4 -C.sub.20)aryl and (C.sub.3 -C.sub.20)cycloalkyl and q is from 1 to 12; m is from 1 to 10,000; and p is from 0 to m. The polymer is formed from a stereochemically pure compound.
REFERENCES:
Koppenhoefer et al. J. Chromatog. 358:159 (1986).
Hemmerle et al. Tetrahedron Lett. 28:3471 (1987).
Ramos Tombo et al. Tetrahedron Lett. 24:5707 (1986).
Huang et al. J. Am. Chem. Soc. 97:14 (1975).
Ohno et al. J. Am. Chem. Soc. 103:2405 (1981).
Chen et al. J. Am. Chem. Soc. 103:3580 (1981).
Cambou et al. J. Am. Chem. Soc. 106:2687 (1984).
Zaks et al. Science 224:1249 (1984).
Gatfield, Annals N.Y. Acad. Sci. 568 (1984).
Zaks et al, PNAS (USA) 82:3192 (1985).
Klibanov, CHEMTECH 354 (1986).
Cambou et al. Biotechnology and Bioengineering 26:1449 (1984).
Kirchner et al. J. Am. Chem. Soc. 107:7072 (1985).
Langrand et al. Tetrahedron Lett. 26:1857 (1985).
Langrand et al. Tetrahedron Lett. 27:29 (1986).
Gil et al. Tetrahedron Lett. 28:1647 (1987).
Bianchi et al. J. Org. Chem. 53:5531 (1988).
Francalanci et al. J. Org. Chem. 52:5079 (1987).
Wang, Yf et al., "Extending the Applicability of Esterases of Low Enantioselectivity in Asymmetric Synthesis", Enzymes in Organic Synthesis, Pittman, London pp. 128-145 1985.
D. Bianchi et al., "Anhydrides as Acylating Agents in Lipase-Catalyzed Stereoselective Esterification of Racemic Alcohol", J. Org. Chem., Nd53, pp. 5531-5334, 1988.
Morrow Cary J.
Wallace Joe S.
Nutter Nathan M.
University of New Mexico
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