Effects of deuterium substitution on the rates of organic reactions. XI. .alpha.- and .beta.-Deuterium effects on the solvolysis rates of a series of substituted 1-phenylethyl halides

V. J. Shiner; W. E. Buddenbaum; B. L. Murr; G. Lamaty

doi:10.1021/ja01004a037

Effects of deuterium substitution on the rates of organic reactions. XI. .alpha.- and .beta.-Deuterium effects on the solvolysis rates of a series of substituted 1-phenylethyl halides

Journal of the American Chemical Society ◽

10.1021/ja01004a037 ◽

1968 ◽

Vol 90 (2) ◽

pp. 418-426 ◽

Cited By ~ 55

Author(s):

V. J. Shiner ◽

W. E. Buddenbaum ◽

B. L. Murr ◽

G. Lamaty

Keyword(s):

Organic Reactions ◽

Deuterium Substitution ◽

Substituted 1

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The Effects of Deuterium Substitution on the Rates of Organic Reactions. VI. Secondary Isotope Effects on the Solvolysis Rates of γ-Methyl Substituted t-Alkyl Chlorides1

Journal of the American Chemical Society ◽

10.1021/ja01462a047 ◽

1961 ◽

Vol 83 (1) ◽

pp. 240-243 ◽

Cited By ~ 6

Author(s):

V. J. Shiner

Keyword(s):

Isotope Effects ◽

Organic Reactions ◽

Deuterium Substitution

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The Effects of Deuterium Substitution on the Rates of Organic Reactions. IV.1Solvolysis of R-Deuteroalkyl Benzhydryl Chlorides2

Journal of the American Chemical Society ◽

10.1021/ja01559a036 ◽

1957 ◽

Vol 79 (2) ◽

pp. 373-375 ◽

Cited By ~ 13

Author(s):

V. J. Shiner ◽

C. J. Verbanic

Keyword(s):

Organic Reactions ◽

Deuterium Substitution

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The Effects of Deuterium Substitution on the Rates of Organic Reactions. III.1,2Solvolysis Rates and Arrhenius Parameters for 2,3-Dimethyl-2-chlorobutane and its 3-Deutero Analog

Journal of the American Chemical Society ◽

10.1021/ja01635a041 ◽

1954 ◽

Vol 76 (6) ◽

pp. 1603-1606 ◽

Cited By ~ 30

Author(s):

V. J. Shiner

Keyword(s):

Organic Reactions ◽

Arrhenius Parameters ◽

Deuterium Substitution ◽

Deutero Analog

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The Effects of Deuterium Substitution on the Rates of Organic Reactions. V. Hydrolysis of α-Deutero Ketals1

Journal of the American Chemical Society ◽

10.1021/ja01570a080 ◽

1957 ◽

Vol 79 (13) ◽

pp. 3599-3602 ◽

Cited By ~ 10

Author(s):

V. J. Shiner ◽

Sally Cross

Keyword(s):

Organic Reactions ◽

Deuterium Substitution ◽

Hydrolysis Of

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The Effects of Deuterium Substitution on the Rates of Organic Reactions. VII. Secondary Effects on the Solvolysis of 3-Halo-3-methyl-1-butynes

Journal of the American Chemical Society ◽

10.1021/ja00871a026 ◽

1962 ◽

Vol 84 (12) ◽

pp. 2408-2411 ◽

Cited By ~ 5

Author(s):

V. J. Shiner ◽

Joseph W. Wilson ◽

Guenther. Heinemann ◽

Norman. Solliday

Keyword(s):

Organic Reactions ◽

Secondary Effects ◽

Deuterium Substitution

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The Effects of Deuterium Substitution on the Rates of Organic Reactions. X. The Solvolyses of 4-Chloro-4-methyl-2-pentyne and Its Deuterated Analogs

Journal of the American Chemical Society ◽

10.1021/ja01067a025 ◽

1964 ◽

Vol 86 (13) ◽

pp. 2643-2645 ◽

Cited By ~ 8

Author(s):

V. J. Shiner ◽

George S. Kriz

Keyword(s):

Organic Reactions ◽

Deuterium Substitution

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Additions and Corrections-The Effects of Deuterium Substitution on the Rates of Organic Reactions. VI. Secondary Isotope Effects on the Solvolysis Rates of γ-Methyl Substituted t-Alkyl Chlorides

Journal of the American Chemical Society ◽

10.1021/ja01485a618 ◽

1961 ◽

Vol 83 (24) ◽

pp. 5049-5049

Author(s):

V Shiner, Jr

Keyword(s):

Isotope Effects ◽

Organic Reactions ◽

Deuterium Substitution

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Catalysis of Organic Reactions Edited by Michael E. Ford (Air Products and Chemicals, Allentown, PA). Marcel Dekker: New York and Basel. 2000. xxvi + 630 pp. $195. ISBN 0-8247-0486-X.

Journal of the American Chemical Society ◽

10.1021/ja004844u ◽

2001 ◽

Vol 123 (7) ◽

pp. 1546-1546

Keyword(s):

New York ◽

Organic Reactions

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Metal catalysis in organic reactions. 18. Stereochemistry of the transition-metal catalyzed cross-coupling of (S)-1-bromo-3-methyl-1,2-pentadiene with isobutylmetal compounds.

Tetrahedron Letters ◽

10.1016/s0040-4039(00)84178-7 ◽

1986 ◽

Vol 29 (9) ◽

pp. 1067-1068

Author(s):

A Caporusso

Keyword(s):

Transition Metal ◽

Cross Coupling ◽

Organic Reactions ◽

Metal Catalysis ◽

Transition Metal Catalyzed ◽

Metal Catalyzed

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Decarboxylation Reactions in a Photocatalytic Microchip

10.26434/chemrxiv.6683045 ◽

2018 ◽

Author(s):

Kenji Katayama ◽

Momona Seki ◽

Kayoko Tokumitsu ◽

Woon Yong Sohn

Keyword(s):

Reaction Time ◽

Organic Reactions ◽

Light Conditions ◽

High Yields

The photocatalytic microchip was demonstrated as an efficient platform of the photocatalytic organic reactions, which features an easy control of the reaction time and light conditions. We demonstrated the photocatalytic decarboxylation and the following adduct reaction inside the microchip and successfully achieved high yields of the products.

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