Conformational studies of trimethylene s
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H.F. van Woerden; H. Cerfontain; C.H. Green; R.J. Reijerkerk
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Article
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1968
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Elsevier Science
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French
⚖ 237 KB
Conformational studies (1,2) of the cyclic sulfites of 2-substituted-propane-1,3-dials have indicated that these esters occupy preferentially a chair form with axial S=O bond. X-ray analyses (3,4) of two compounds have shown that the sulfite group holds the remainder of the ring in au almost ideal s