Standout Papers

Rapid reaction of representative olefins with monochloroborane diethyl etherate. Simple, con... 1972 2026 1990 2008 42
  1. Rapid reaction of representative olefins with monochloroborane diethyl etherate. Simple, convenient synthesis of dialkylchloroboranes and dialkylborinic acid derivatives (1972)
    Herbert C. Brown, N. RAVINDRAN Journal of the American Chemical Society
  2. Reaction of representative olefins with dichloroborane ethyl etherate induced by boron trichloride. Exceptionally simple, general synthesis of alkyldichloroboranes and alkylboronic acid derivatives via hydroboration (1973)
    Herbert C. Brown, N. RAVINDRAN Journal of the American Chemical Society
  3. Hydroboration. XLI. Hydroboration of alkenes and alkynes with dichloroborane etherates. Convenient procedures for the preparation of alkyl- and alkenyldichloroboranes and their derivatives (1976)
    Herbert C. Brown, N. RAVINDRAN Journal of the American Chemical Society
  4. Monobromoborane: Dimethyl Sulfide; A New Stable Reagent for Hydroboration, Providing a General Synthesis of Dialkylbromoboranes and their Derivatives (1977)
    Herbert C. Brown, N. RAVINDRAN Synthesis
  5. Hydroboration. 52. Monohaloborane-methyl sulfide adducts as new reagents for the hydroboration of alkenes. A convenient synthesis of dialkylhaloboranes and their derivatives for organic synthesis (1979)
    Herbert C. Brown, N. RAVINDRAN et al. The Journal of Organic Chemistry
  6. Reaction of alkenylboronic acids with iodine under the influence of base. Simple procedure for the stereospecific conversion of terminal alkynes into trans-1-alkenyl iodides via hydroboration (1973)
    Herbert C. Brown, Tsutomu Hamaoka et al. Journal of the American Chemical Society
  7. Stereospecific conversion of alkenylboronic acids into alkenyl bromides with inversion of configuration. Striking differences in the stereochemistry of the replacement of the boronic acid substituent by bromine and iodine and its significance in terms of the reaction mechanism (1973)
    Herbert C. Brown, Tsutomu Hamaoka et al. Journal of the American Chemical Society
  8. Hydroboration. XL. Hydroboration of alkenes and alkynes with monochloroborane etherates. Convenient procedures for the preparation of dialkyl-, monoalkyl-, and dialkenylchloroboranes and their derivatives (1976)
    Herbert C. Brown, N. RAVINDRAN Journal of the American Chemical Society
  9. Molecular addition compounds. 3. Redistribution of borane-methyl sulfide with boron trichloride-methyl sulfide and boron tribromide-methyl sulfide as convenient routes to the corresponding haloborane-methyl sulfides (1977)
    Herbert C. Brown, N. RAVINDRAN Inorganic Chemistry
  10. Reaction of representative alkynes with monochloroborane diethyl etherate. Simple convenient synthesis of dialkenylchloroboranes via hydroboration (1973)
    Herbert C. Brown, N. RAVINDRAN The Journal of Organic Chemistry
  11. Unusually powerful directive effect in the hydroboration of representative olefins with monochloroborane-ethyl etherate (1973)
    Herbert C. Brown, N. RAVINDRAN The Journal of Organic Chemistry
  12. Monochloroborane-methyl sulfide, H2BCl.S(CH3)2, and dichloroborane-methyl sulfide, HBCl2.S(CH3)2, as new stable hydroborating agents with high regiospecificity (1977)
    Herbert C. Brown, N. RAVINDRAN The Journal of Organic Chemistry
  13. The reaction of alkynes with dichloroborane ethyl etherate in the presence of boron trichloride. A simple, general synthesis of alkenyldichloroboranes (1973)
    Herbert C. Brown, N. RAVINDRAN Journal of Organometallic Chemistry
  14. Direct reaction of dibromoborane-methyl sulfide, HBBr2.cntdot.S(CH3)2, with alkenes. The remarkable reactivity of dibromoborane-methyl sulfide as a hydroborating agent as compared with related dichloroborane derivatives (1977)
    Herbert C. Brown, N. RAVINDRAN Journal of the American Chemical Society

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Works of N. RAVINDRAN being referenced

An Exceptionally Rapid and Selective Deoxygenation of Aliphatic Sulfoxides to Sulfides under Mild Conditions with a New Reducing Agent, Dichloroborane
2002 Nobel
Reaction of alkenylboronic acids with iodine under the influence of base. Simple procedure for the stereospecific conversion of terminal alkynes into trans-1-alkenyl iodides via hydroboration
1973 StandoutNobel
Unusually powerful directive effect in the hydroboration of representative olefins with monochloroborane-ethyl etherate
1973 StandoutNobel
Reaction of representative alkynes with monochloroborane diethyl etherate. Simple convenient synthesis of dialkenylchloroboranes via hydroboration
1973 StandoutNobel
Direct reaction of dibromoborane-methyl sulfide, HBBr2.cntdot.S(CH3)2, with alkenes. The remarkable reactivity of dibromoborane-methyl sulfide as a hydroborating agent as compared with related dichloroborane derivatives
1977 StandoutNobel
The reaction of alkynes with dichloroborane ethyl etherate in the presence of boron trichloride. A simple, general synthesis of alkenyldichloroboranes
1973 StandoutNobel
Rapid reaction of representative olefins with monochloroborane diethyl etherate. Simple, convenient synthesis of dialkylchloroboranes and dialkylborinic acid derivatives
1972 StandoutNobel
Stereospecific conversion of alkenylboronic acids into alkenyl bromides with inversion of configuration. Striking differences in the stereochemistry of the replacement of the boronic acid substituent by bromine and iodine and its significance in terms of the reaction mechanism
1973 StandoutNobel
Hydroboration. XLI. Hydroboration of alkenes and alkynes with dichloroborane etherates. Convenient procedures for the preparation of alkyl- and alkenyldichloroboranes and their derivatives
1976 StandoutNobel
Hydroboration. 52. Monohaloborane-methyl sulfide adducts as new reagents for the hydroboration of alkenes. A convenient synthesis of dialkylhaloboranes and their derivatives for organic synthesis
1979 StandoutNobel
Hydroboration. XL. Hydroboration of alkenes and alkynes with monochloroborane etherates. Convenient procedures for the preparation of dialkyl-, monoalkyl-, and dialkenylchloroboranes and their derivatives
1976 StandoutNobel
Vinylic organoboranes. 13. A convenient stereospecific synthesis of (Z)-1-halo-1-alkenes from 1-alkynes via (E)-1-alkenylborane derivatives with halogens
1989 Nobel
Monochloroborane-methyl sulfide, H2BCl.S(CH3)2, and dichloroborane-methyl sulfide, HBCl2.S(CH3)2, as new stable hydroborating agents with high regiospecificity
1977 StandoutNobel
Reaction of representative olefins with dichloroborane ethyl etherate induced by boron trichloride. Exceptionally simple, general synthesis of alkyldichloroboranes and alkylboronic acid derivatives via hydroboration
1973 StandoutNobel
Vinylic organoboranes. 14. A stereospecific synthesis of (E)-1-halo-1-alkenes from 1-alkynes
1989
Molecular addition compounds. 3. Redistribution of borane-methyl sulfide with boron trichloride-methyl sulfide and boron tribromide-methyl sulfide as convenient routes to the corresponding haloborane-methyl sulfides
1977 StandoutNobel
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