Standout Papers

Forty years of hydride reductions 1972 2026 1990 2008 355
  1. Forty years of hydride reductions (1979)
    Herbert C. Brown, S. Krishnamurthy Tetrahedron
  2. Lithium .beta.-isopinocamphenyl-9-borabicyclo[3.3.1]nonyl hydride. A new reagent for the asymmetric reduction of ketones with remarkable consistency (1977)
    S. Krishnamurthy, Herbert C. Brown et al. The Journal of Organic Chemistry
  3. Selective reductions. 25. Remarkably facile reductive opening of cyclic ethers by the lithium tri-tert-butoxyaluminohydride-triethylborane combination (1979)
    S. Krishnamurthy, Herbert C. Brown The Journal of Organic Chemistry
  4. Addition compounds of alkali metal hydrides (1979)
    Herbert C. Brown, S. Krishnamurthy et al. Journal of Organometallic Chemistry
  5. Lithium tri-sec-butylborohydride. New reagent for the reduction of cyclic and bicyclic ketones with super stereoselectivity. Remarkably simple and practical procedure for the conversion of ketones to alcohols in exceptionally high stereochemical purity (1972)
    Herbert C. Brown, S. Krishnamurthy Journal of the American Chemical Society
  6. Lithium triethylborohydride. Exceptionally powerful nucleophile in displacement reactions with organic halides (1973)
    Herbert C. Brown, S. Krishnamurthy Journal of the American Chemical Society
  7. Selective reductions. XXI. 9-Borabicyclo[3.3.1]nonane in tetrahydrofuran as a new selective reducing agent in organic synthesis. Reaction with selected organic compounds containing representative functional groups (1976)
    Herbert C. Brown, S. Krishnamurthy et al. The Journal of Organic Chemistry
  8. Addition compounds of alkali metal hydrides. 15. Steric effects in the reaction of representative trialkylboranes with lithium and sodium hydrides to form the corresponding trialkylborohydrides (1978)
    Herbert C. Brown, S. Krishnamurthy et al. Journal of the American Chemical Society
  9. Addition compounds of alkali metal hydrides. 14. The reaction of trialkylboranes with lithium trialkylborohydrides (1977)
    Herbert C. Brown, S. Krishnamurthy et al. Journal of the American Chemical Society
  10. Lithium triethylborohydride as a convenient reagent for the facile reduction of both hindered and bicyclic epoxides prone to electrophilically induced rearrangement (1973)
    S. Krishnamurthy, Herbert C. Brown et al. Journal of the American Chemical Society
  11. Lithium triethylborohydride and monomeric aluminium t-butoxide as the active intermediates in the reductive opening of tetrahydrofuran and related ethers by the triethylborane induced reaction of lithium tri-t-butoxyaluminohydride (1972)
    Herbert C. Brown, S. Krishnamurthy Journal of the Chemical Society Chemical Communications
  12. Lithium trisiamylborohydride. A new sterically hindered reagent for the reduction of cyclic ketones with exceptional stereoselectivity (1976)
    S. Krishnamurthy, Herbert C. Brown Journal of the American Chemical Society
  13. 9-Borabicyclo[3.3.1]nonane as a highly selective reducing agent for the facile conversion of .alpha.,.beta.-unsaturated aldehydes and ketones to the corresponding allylic alcohols in the presence of other functional groups (1975)
    S. Krishnamurthy, Herbert C. Brown The Journal of Organic Chemistry
  14. Selective reductions. XIV. Fast reaction of aryl bromides and iodides with lithium aluminum hydride in tetrahydrofuran. Simple convenient procedure for the hydrogenolysis of aryl bromides and iodides (1969)
    Herbert C. Brown, S. Krishnamurthy The Journal of Organic Chemistry
  15. Remarkably facile reductive opening of tetrahydrofuran and related ethers by lithium tri-tert-butoxyaluminohydride in the presence of triethylborane (1972)
    Herbert C. Brown, S. Krishnamurthy et al. Journal of the American Chemical Society
  16. Addition compounds of alkali metal hydrides (1979)
    Herbert C. Brown, S. Krishnamurthy et al. Journal of Organometallic Chemistry
  17. Facile reduction of alkyl tosylates with lithium triethylborohydride. An advantageous procedure for the deoxygenation of cyclic and acyclic alcohols (1976)
    S. Krishnamurthy, Herbert C. Brown The Journal of Organic Chemistry
  18. Selective reductions. 22. Facile reduction of .alpha.,.beta.-unsaturated aldehydes and ketones with 9-borabicyclo[3.3.1]nonane. A remarkably convenient procedure for the selective conversion of conjugated aldehydes and ketones to the corresponding allylic alcohols in the presence of other functional groups (1977)
    S. Krishnamurthy, Herbert C. Brown The Journal of Organic Chemistry

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Works of S. Krishnamurthy being referenced

Selective reductions. XIV. Fast reaction of aryl bromides and iodides with lithium aluminum hydride in tetrahydrofuran. Simple convenient procedure for the hydrogenolysis of aryl bromides and iodides
1969 StandoutNobel
Low molecular weight chelators and phenolic compounds isolated from wood decay fungi and their role in the fungal biodegradation of wood1This is paper 2084 of the Maine Agricultural and Forest Experiment Station.1
1997
Selective reductions. XIX. Rapid reaction of carboxylic acids with borane-tetrahydrofuran. Remarkably convenient procedure for the selective conversion of carboxylic acids to the corresponding alcohols in the presence of other functional groups
1973
Forty years of hydride reductions
1979 StandoutNobel
Lithium trisiamylborohydride. A new sterically hindered reagent for the reduction of cyclic ketones with exceptional stereoselectivity
1976 StandoutNobel
ChemInform Abstract: 9‐BORABICYCLO(3.3.1)NONANE AS A HIGHLY SELECTIVE REDUCING AGENT FOR THE FACILE CONVERSION OF ALPHA,BETA‐UNSATURATED ALDEHYDES AND KETONES TO THE CORRESPONDING ALLYLIC ALCOHOLS IN THE PRESENCE OF OTHER FUNCTIONAL GROUPS
1975
Lithium triethylborohydride. Exceptionally powerful nucleophile in displacement reactions with organic halides
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Selective reductions. 27. Reaction of alkyl halides with representative complex metal hydrides and metal hydrides. Comparison of various hydride reducing agents
1980 Nobel
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2003
Selective reductions. 26. Lithium triethylborohydride as an exceptionally powerful and selective reducing agent in organic synthesis. Exploration of the reactions with selected organic compounds containing representative functional groups
1980 Nobel
Lithium tris(3-ethyl-3-pentyloxy)aluminohydride. A new remarkably chemoselective reagent for the reduction of aldehydes in the presence of ketones
1981
Hydrodeoxygenation of dibenzofuran and related compounds
1981
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1975 StandoutNobel
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1982
Lithium triethylborohydride as a convenient reagent for the facile reduction of both hindered and bicyclic epoxides prone to electrophilically induced rearrangement
1973 StandoutNobel
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1972 StandoutNobel
Selective reductions. 28. The fast reaction of lithium aluminum hydride with alkyl halides in tetrahydrofuran. A reappraisal of the scope of the reaction
1982 Nobel
Selective reductions. XXI. 9-Borabicyclo[3.3.1]nonane in tetrahydrofuran as a new selective reducing agent in organic synthesis. Reaction with selected organic compounds containing representative functional groups
1976 StandoutNobel
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