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Скачайте пожалуйста статьи:
1. Organoborane-carbon monoxide reactions. Synthesis of carbon structures
Herbert Charles Brown
Acc. Chem. Res., 1969, 2 (3), pp 65–72

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http://dx.doi.org/10.1021/ar50015a001

2. New selective reducing agents
Herbert C. Brown
J. Chem. Educ., 1961, 38 (4), p 173

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http://dx.doi.org/10.1021/ed038p173

3. Improved Procedures for the Generation of Diborane from Sodium Borohydride and Boron Trifluoride
Josyula V. B. Kanth and Herbert C. Brown
Inorg. Chem., 2000, 39 (8), pp 1795–1802

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http://dx.doi.org/10.1021/ic0000911

4. Molecular addition compounds. 9. Effect of structure on the reactivities of representative borane-amine complexes in typical reactions such as hydrolysis, hydroboration, and reduction
Herbert C. Brown, Leo T. Murray
Inorg. Chem., 1984, 23 (18), pp 2746–2753

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http://dx.doi.org/10.1021/ic00186a008

5. Convenient procedure for the conversion of sodium borohydride into lithium borohydride in simple ether solvents
Herbert C. Brown, Yong Moon. Choi, S. Narasimhan
Inorg. Chem., 1981, 20 (12), pp 4454–4456

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http://dx.doi.org/10.1021/ic50226a091

6. Molecular addition compounds. 7. Synthesis of addition compounds of boron trifluoride, borane, and alane with N,N,N'N'-tetramethylethylenediamine and triethylenediamine by precipitation from ether solvents
Herbert C. Brown, Bakthan Singaram
Inorg. Chem., 1980, 19 (2), pp 455–457

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http://dx.doi.org/10.1021/ic50204a034

7. Molecular addition compounds. 6. Addition compounds of ethylenediamine with boron trifluoride and dialkylboranes
Herbert C. Brown, Bakthan Singaram
Inorg. Chem., 1979, 18 (1), pp 53–55

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http://dx.doi.org/10.1021/ic50191a011

8. Molecular addition compounds. 5. Interaction of N,N,N',N',-tetramethylethylenediamine with boron trifluoride and monoalkylboranes
Herbert C. Brown, Bakthan Singaram, John R. Schwier
Inorg. Chem., 1979, 18 (1), pp 51–53

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http://dx.doi.org/10.1021/ic50191a010

9. Addition compounds of alkali metal hydrides. 13. Reactions of alkali metal hydrides with trialkylboranes. Synthesis and dissociation of alkali metal trialkylborohydrides. Ethyl ether-organoborane as a reversible "solvent" for lithium hydride
Herbert C. Brown, Albert. Khuri, S. C. Kim
Inorg. Chem., 1977, 16 (9), pp 2229–2233

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http://dx.doi.org/10.1021/ic50175a015

10. Organoboranes. II. The Preparation and Properties of Alkyldiboranes Containing Bulky Alkyl Substituents
Herbert C. Brown, Gerald J. Klender
Inorg. Chem., 1962, 1 (2), pp 204–214

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http://dx.doi.org/10.1021/ic50002a003

Большое спасибо!

[macro]

4-10

[macro]

1,3

[suprachemister]

2

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http://upload.com.ua/get/901677393/