C. F. Lane

发表

SODIUM CYANOBOROHYDRIDE ‐ A HIGHLY SELECTIVE REDUCING AGENT FOR ORGANIC FUNCTIONAL GROUPS

C. F. Lane, 1975 .

Organic synthesis using borane-methyl sulfide. Hydroboration-oxidation of alkenes

C. F. Lane, 1974 .

Organoboranes for synthesis. 10.1 the base-induced reaction of bromine with organoboranes. A convenient procedure for the conversion of alkenes into alkyl bromides via hydroboration

H. Brown, C. F. Lane, 1988 .

Thermochemistry for the dehydrogenation of methyl-substituted ammonia borane compounds.

D. Dixon, D. Camaioni, M. H. Matus, 2009, The journal of physical chemistry. A.

SODIUM CYANOBOROHYDRIDE ‐ A HIGHLY SELECTIVE REDUCING AGENT FOR ORGANIC FUNCTIONAL GROUPS

C. F. Lane, 1975 .

Catecholborane: A new hydroboration reagent

G. Kabalka, C. F. Lane, 1976 .

Reduction of organic compounds with diborane

C. F. Lane, 1976 .

Organic synthesis using borane-methyl sulfide. II. Reduction of aromatic carboxylic acids in the presence of trimethyl borate

C. F. Lane, J. Daniels, H. Myatt, 1974 .

Base-induced bromination of tri-exo-norbornylborane: an electrophilic substitution with predominant inversion of configuration

H. Brown, C. F. Lane, 1971 .

Light-induced reaction of bromine with trialkylboranes in the presence of water. A remarkably simple procedure for the union of two or three alkyl groups to produce highly substituted alcohols

H. Brown, C. F. Lane, 1971 .

Formation of alkyl bromides in the dark reaction of bromine with organoboranes. Evidence for an unusual pathway involving the prior bromination of the organoborane

H. Brown, C. F. Lane, 1970 .

ORGANIC SYNTHESIS VIA BROMINATION OF ORGANOBORANES

C. F. Lane, 1974 .

The Light-Induced Reaction of Dialkylborinic Acids with Bromine in the Presence of Water. An Unusually Simple Procedure for the Synthesis of Highly Substituted Tertiary Alcohols

H. Brown, C. F. Lane, 1972 .

The Light-Induced Reaction of Thexyldialkylboranes with Bromine in the Presence of Water. A New and Convenient Synthesis of Tertiary Alcohols Including Those Containing Functional Substituents

H. Brown, Yoshinori Yamamoto, C. F. Lane, 1972 .

Base-induced reaction of organoboranes with bromine. Convenient procedure for the anti-Markovnikov hydrobromination of terminal olefins via hydroboration-bromination

H. Brown, C. F. Lane, 1970 .

The reaction between trialkylboranes and copper(II) salts. An unusual electron-transfer oxidation-reduction

C. F. Lane, 1971 .

Selective Reductions Using Metal Hydrides

C. F. Lane, 1978 .

Organoboranes for synthesis. 11.1 preparation of alkyl bromides in the dark reaction of bromine with organoboranes2,3 exceptional reactivity toward radical bromination of the alpha hydrogen in trialkylboranes

H. Brown, C. F. Lane, N. D. Lue, 1988 .

Synthesis of secondary alkyl bromides in the dark reaction of bromine with B-sec-alkyl-9-borabicyclo[3.3.1]nonanes. A convenient procedure for the anti-Markovnikov hydrobromination of internal olefins

H. Brown, C. F. Lane, 1971 .

The facile displacement of 2,3-dimethyl-2-butene in the reaction of bulky olefins with thexylcycloalkylboranes. A convenient synthetic route to certain mixed organoboranes

H. Brown, C. F. Lane, 1972 .

Sodium Cyanoborohydride - A Highly Selective Reducing Agent for Organic Functional Groups

C. F. Lane, 1975 .