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Green, Mark M., Reidy, Michael P., Johnson, Robert D., Darling, Graham, O'Leary, Daniel J., Willson, Grant (1989) Macromolecular stereochemistry: the out-of-proportion influence of optically active comonomers on the conformational characteristics of polyisocyanates. The sergeants and soldiers experiment. Journal Of The American Chemical Society, 111 (16) 6452-6454 doi:10.1021/ja00198a084

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Reference TypeJournal (article/letter/editorial)
TitleMacromolecular stereochemistry: the out-of-proportion influence of optically active comonomers on the conformational characteristics of polyisocyanates. The sergeants and soldiers experiment
JournalJournal Of The American Chemical Society
AuthorsGreen, Mark M.Author
Reidy, Michael P.Author
Johnson, Robert D.Author
Darling, GrahamAuthor
O'Leary, Daniel J.Author
Willson, GrantAuthor
Year1989 (August)Volume111
Issue16
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00198a084Search in ResearchGate
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Mindat Ref. ID1434090Long-form Identifiermindat:1:5:1434090:9
GUID0
Full ReferenceGreen, Mark M., Reidy, Michael P., Johnson, Robert D., Darling, Graham, O'Leary, Daniel J., Willson, Grant (1989) Macromolecular stereochemistry: the out-of-proportion influence of optically active comonomers on the conformational characteristics of polyisocyanates. The sergeants and soldiers experiment. Journal Of The American Chemical Society, 111 (16) 6452-6454 doi:10.1021/ja00198a084
Plain TextGreen, Mark M., Reidy, Michael P., Johnson, Robert D., Darling, Graham, O'Leary, Daniel J., Willson, Grant (1989) Macromolecular stereochemistry: the out-of-proportion influence of optically active comonomers on the conformational characteristics of polyisocyanates. The sergeants and soldiers experiment. Journal Of The American Chemical Society, 111 (16) 6452-6454 doi:10.1021/ja00198a084
In(1989, August) Journal Of The American Chemical Society Vol. 111 (16) American Chemical Society (ACS)

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Lifson, S., Green, Mark M., Andreola, C., Peterson, N. C. (1989) Macromolecular stereochemistry: helical sense preference in optically active polyisocyanates. Amplification of a conformational equilibrium deuterium isotope effect. Journal Of The American Chemical Society, 111 (24) 8850-8858 doi:10.1021/ja00206a013
Green, Mark M., Andreola, Christopher., Munoz, Beth., Reidy, Michael P., Zero, Karl. (1988) Macromolecular stereochemistry: a cooperative deuterium isotope effect leading to a large optical rotation. Journal Of The American Chemical Society, 110 (12) 4063-4065 doi:10.1021/ja00220a070
Green, Mark M., Gross, Richard A., Crosby, Charles, Schilling, Frederic C. (1987) Macromolecular stereochemistry: the effect of pendant group structure on the axial dimension of polyisocyanates. Macromolecules, 20. 992-999 doi:10.1021/ma00171a019
Cook, Robert, Johnson, Robert D., Wade, C. G., O'Leary, Daniel J., Munoz, Beth, Green, Mark M. (1990) Solvent dependence of the chain dimensions of poly(n-hexyl isocyanate). Macromolecules, 23. 3454-3458 doi:10.1021/ma00216a012
Burwell, Robert L. (1949) The Stereochemistry of the Sulfation of Optically Active Secondary Butyl Alcohol. Journal Of The American Chemical Society, 71 (5) 1769-1771 doi:10.1021/ja01173a067
Reidy, Michael P., Green, Mark M. (1990) Macromolecular stereochemistry of poly(p-biphenylmethyl-L-glutamate): linkage between biphenyl twist sense and polypeptide conformation and observation of microaggregation-driven, sudden, temperature-dependent chiral optical changes. Macromolecules, 23. 4225-4234 doi:10.1021/ma00221a008
Cobos, Katherine, Rodríguez, Rafael, Quiñoá, Emilio, Riguera, Ricardo, Freire, Félix (2020) From Sergeants and Soldiers to Chiral Conflict Effects in Helical Polymers by Acting on the Conformational Composition of the Comonomers. Angewandte Chemie, 132 (52) 23932-23938 doi:10.1002/ange.202009215
Streitwieser, A., Wolfe, J. R. (1959) Stereochemistry of the Primary Carbon. XI. Ethanolysis of Optically Active Benzyl-α-d p-Toluenesulfonate1. Journal Of The American Chemical Society, 81 (18) 4912-4914 doi:10.1021/ja01527a038
Sommer, L. H., Michael, K. W., Korte, W. D. (1963) Stereochemistry of Asymmetric Silicon: Synthesis, Stereochemistry, and Absolute Configurations of New Optically Active Organosilicon Systems. Journal Of The American Chemical Society, 85 (22) 3712-3713 doi:10.1021/ja00905a050
Anderson, Robert Charles, Fraser-Reid, Bert (1975) Synthesis of optically active avenaciolide from D-glucose. Correct stereochemistry of the natural product. Journal Of The American Chemical Society, 97 (13) 3870-3871 doi:10.1021/ja00846a081
Sita, Lawrence R., Bickerstaff, Richard D. (1989) 2,2,4,4,5,5-Hexakis(2,6-diethylphenyl)pentastanna[1.1.1]propellane: characterization and molecular structure. Journal Of The American Chemical Society, 111 (16) 6454-6456 doi:10.1021/ja00198a085
 
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