21 results on '"Roger Robert"'
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2. 301.—Studies in stereochemical structure. Part IV. Esters of (–)menthol and the (–), (+), and r-mandelic acids
3. 336. Studies in stereochemical structure. Part VII. The rotatory powers and racemisations of the optically active benzoins
4. 220. Studies in stereochemical structure. Part VIII. The stereochemical relationship of the α- and the β-forms of substituted hydrobenzoins. (a) Ethylhydrobenzoin (α-form)
5. Studies in stereochemical structure. Part XI. Heterocyclic compounds from benzoin
6. CII.—Migration of groups in derivatives of benzoin and desylamine
7. 23. Studies in stereochemical structure. Part IX. The stereochemical relationship of the α- and the β-forms of substituted hydrobenzoins. (b) ethylhydrobenzoin (β-form)
8. Elimination of water from glycols. Dehydration of racemic 1 : 4-glycols derived from acenaphthene
9. 367. The dehydration of r-2-phenyl-1-o-, -m-, and -p-tolyl-1-ethyl-ethylene glycols (α-forms)
10. 129. Studies in stereochemical structure. Part XIII. Derivatives of the hydratropic acids and hydratropic alcohols
11. 88. The dehydration of the α-forms of r- and (+)-o- and -m-tolylhydrobenzoins
12. 408. The action of grignard reagents on desyl chloride. Part I. Aryl grignard reagents
13. LXXXVI.—Elimination of the amino-group of tertiary amino-alcohols. Part IV. The displacement of the amino- by the hydroxy-group
14. 385. The dehydration of the α-forms of r- and (+)-p-tolylhydrobenzoins
15. Note
16. CCCIV.—Studies in stereochemical structure. Part III. Glycols derived from d(—)-mandelic acid
17. 622. Studies in stereochemical structure. Part XIV. The resolution of α-hydroxy-amidinium chlorides by the use of mandelic acids
18. CCLXXXIV.—The dehydration of the optically active methyl- and ethyl-hydrobenzoins
19. CVI.—Elimination of the amino-group of tertiary amino-alcohols. Part III. A new method for the preparation of optically active ketones
20. 102. The synthesis of substituted benzoins and of deoxybenzoins
21. 35. Studies in stereochemical structure. Part VI. The isomeric (–)menthyl α-naphthylglycollates
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