Leaving group effects in thiolester hydrolysis. Part 2. On the possibility of an elimination–addition (keten) mediated pathway in S-acetylcoenzyme a basic hydrolysis and acetyl transfer

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/p29810000171 ◽

1981 ◽

pp. 171-174 ◽

Cited By ~ 4

Author(s):

Kenneth T. Douglas ◽

Norbert F. Yaggi ◽

Cynthia M. Mervis

Keyword(s):

Leaving Group ◽

Basic Hydrolysis ◽

Acetyl Transfer ◽

Group Effects

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ChemInform Abstract: LEAVING GROUP EFFECTS IN THIOLESTER HYDROLYSIS. PART 2. ON THE POSSIBILITY OF F AN ELIMINATION-ADDITION (KETEN) MEDIATED PATHWAY IN S-ACETYLCOENZYME A BASIC HYDROLYSIS AND ACETYL TRANSFER

Chemischer Informationsdienst ◽

10.1002/chin.198113174 ◽

1981 ◽

Vol 12 (13) ◽

Author(s):

K. T. DOUGLAS ◽

N. F. YAGGI ◽

C. M. MERVIS

Keyword(s):

Leaving Group ◽

Basic Hydrolysis ◽

Acetyl Transfer ◽

Group Effects

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ChemInform Abstract: LEAVING GROUP EFFECTS IN THIOL ESTER ALKALINE HYDROLYSIS. PART 1. A KETENE-MEDIATED (E1CB) PATH FOR BASIC HYDROLYSIS OF S-ACETOACETYLCOENZYME A AND ANALOGS

Chemischer Informationsdienst ◽

10.1002/chin.198038103 ◽

1980 ◽

Vol 11 (38) ◽

Author(s):

K. T. DOUGLAS ◽

N. F. YAGGI

Keyword(s):

Alkaline Hydrolysis ◽

Thiol Ester ◽

Leaving Group ◽

Basic Hydrolysis ◽

Hydrolysis Of ◽

Group Effects

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Leaving group effects in thiolester alkaline hydrolysis. Part 1. A keten-mediated (E1 cB) pathway for basic hydrolysis of S-acetoacetylcoenzyme A and analogues

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/p29800001037 ◽

1980 ◽

pp. 1037 ◽

Cited By ~ 10

Author(s):

Kenneth T. Douglas ◽

Norbert F. Yaggi

Keyword(s):

Alkaline Hydrolysis ◽

Leaving Group ◽

Basic Hydrolysis ◽

Hydrolysis Of ◽

Group Effects

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ChemInform Abstract: Kinetic and Spectroscopic Characterization of Highly Reactive Methanesulfonates (I)-(IV). Leaving Group Effects for Solvolyses and Comments on Geminal Electronic Effects Influencing SN1 Reactivity.

ChemInform ◽

10.1002/chin.199519050 ◽

2010 ◽

Vol 26 (19) ◽

pp. no-no

Author(s):

T. W. BENTLEY ◽

M. CHRISTL ◽

R. KEMMER ◽

G. LLEWELLYN ◽

J. E. OAKLEY

Keyword(s):

Spectroscopic Characterization ◽

Electronic Effects ◽

Leaving Group ◽

Group Effects

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ChemInform Abstract: Nucleophilic Substitution at a Trigonal Carbon. Part 6. Substituent and Bromide/Chloride Leaving Group Effects in the Reactions of Aromatic Acyl Chlorides with Methanol in Acetonitrile.

ChemInform ◽

10.1002/chin.199915031 ◽

2010 ◽

Vol 30 (15) ◽

pp. no-no

Author(s):

Dennis N. Kevill ◽

William F. K. Wang

Keyword(s):

Nucleophilic Substitution ◽

Acyl Chlorides ◽

Leaving Group ◽

Group Effects

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Nucleophilic substitution at a trigonal carbon. Part 6.1 Substituent and bromide/chloride leaving group effects in the reactions of aromatic acyl chlorides with methanol in acetonitrile

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/a806493h ◽

1998 ◽

pp. 2631-2638 ◽

Cited By ~ 7

Author(s):

Dennis N. Kevill ◽

William F. K. Wang

Keyword(s):

Nucleophilic Substitution ◽

Acyl Chlorides ◽

Leaving Group ◽

Group Effects

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Leaving Group Effects on the Selectivity of the Silylation of Alcohols: The Reactivity–Selectivity Principle Revisited

Organic Letters ◽

10.1021/acs.orglett.5b01536 ◽

2015 ◽

Vol 17 (13) ◽

pp. 3318-3321 ◽

Cited By ~ 12

Author(s):

Pascal Patschinski ◽

Hendrik Zipse

Keyword(s):

Leaving Group ◽

Selectivity Principle ◽

Group Effects

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Lithium aluminum hydride reduction of allylic substrates. Notable leaving group effects on the product regiochemistry

The Journal of Organic Chemistry ◽

10.1021/jo00195a049 ◽

1984 ◽

Vol 49 (21) ◽

pp. 4084-4086 ◽

Cited By ~ 12

Author(s):

Tomoatsu Hirabe ◽

Masatomo Nojima ◽

Shigekazu Kusabayashi

Keyword(s):

Lithium Aluminum Hydride ◽

Aluminum Hydride ◽

Lithium Aluminum ◽

Hydride Reduction ◽

Leaving Group ◽

Group Effects

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ChemInform Abstract: Leaving-Group Effects on Kinetic Parameters for Solvolysis Reactions of Sterically Hindered Palladium(II) Complexes in Aqueous Solution.

ChemInform ◽

10.1002/chin.198709287 ◽

1987 ◽

Vol 18 (9) ◽

Author(s):

M. KOTOWSKI ◽

R. VAN ELDIK

Keyword(s):

Aqueous Solution ◽

Kinetic Parameters ◽

Leaving Group ◽

Sterically Hindered ◽

Group Effects

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Reverse micelles as a model system with which to study leaving group effects on alkaline phosphatase-catalysed hydrolysis

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/a701918a ◽

1997 ◽

pp. 2757-2760 ◽

Cited By ~ 6

Author(s):

Hui-Chih Hung ◽

Ter-Mei Huang ◽

Gu-Gang Chang

Keyword(s):

Alkaline Phosphatase ◽

Reverse Micelles ◽

Model System ◽

Leaving Group ◽

Group Effects

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