P. G. Wuts

发表

Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

Continuous Flow Homolytic Aromatic Substitution with Electrophilic Radicals: A Fast and Scalable Protocol for Trifluoromethylation.

D. Roberge, C. Kappe, P. F. Carneiro, 2017, Chemistry.

Generation of Broad-Spectrum Antifungal Drug Candidates from the Natural Product Compound Aureobasidin A.

J. Slightom, Brian P. H. Metzger, Å. Elhammer, 2015, ACS medicinal chemistry letters.

PREPARATION OF HALOMETHANEBORONATES

P. G. Wuts, P. Thompson, 1982 .

Stereoselective synthesis of Xaa psi[CH2CH(OH)]Yaa dipeptidomimetics and their inclusion in HIV-1 protease inhibitors.

H. G. Chen, T. Sawyer, C. W. Smith, 2009, International journal of peptide and protein research.

Protection for the Carboxyl Group

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

Dialkylhydrazides for directed orthometalations

P. G. Wuts, M. Goble, S. A. Pratt, 2000 .

Protection for the Amino Group

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2006 .

Protection for the Thiol Group

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

Protection for the Phosphate Group

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

Protection for the Carbonyl Group

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

Stereocontrolled total synthesis of .alpha.- and .beta.-santonin

J. A. Marshall, P. G. Wuts, 1978 .

Thermal and trimethylsilyl triflate catalyzed additions of allylsilanes to nitrones

Yong-woon Jung, P. G. Wuts, 1988 .

Stereoselective synthesis of racemic occidentalol and related cis-fused hexahydronaphthalenes from m-toluic acid

J. A. Marshall, P. G. Wuts, 1977 .

Application of allylboronates to the synthesis of carbomycin B

P. G. Wuts, S. Bigelow, 1988 .

Allylboronate synthesis. Synthesis of a .beta.-alkoxy carbanion equivalent

P. G. Wuts, P. Thompson, Gary R. Callen, 1983 .

PREPARATION OF HALOMETHANEBORONATES

P. G. Wuts, P. Thompson, 1982 .

The Role of Protective Groups in Organic Synthesis

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

Greene's Protective Groups in Organic Synthesis

Theodora W. Greene, Peter G. M. Wuts, P. G. Wuts, 2006 .

2‐Methoxyethoxymethyl Chloride

P. G. Wuts, 2001 .

Asymmetric synthesis of (–)-exo-brevicomin. Chirality transfer from a chiral (tetrahy-dropyranyloxyallyl)boronate in the condensation with aldehydes

P. G. Wuts, S. Bigelow, 1984 .

The addition of .gamma.-(trimethylsilyl)allylboronates to imines

Yong-woon Jung, P. G. Wuts, 1991 .

p‐(Methoxybenzyloxy)methyl Chloride

P. G. Wuts, 2001 .

Hydroformylation as a simple and efficient one carbon homologation of homoallylic alcohols: synthesis of Prelog-Djerassi lactone

P. G. Wuts, M. Obrzut, P. Thompson, 1984 .

An Improved Procedure for the Cr(II) Mediated Homoallylic Alcohol Synthesis

P. G. Wuts, Gary R. Callen, 1986 .

The oxidation of aldehyde bisulfite adducts to carboxylic acids and their derivatives with dimethylsulfoxide and acetic anhydride

P. G. Wuts, C. Bergh, 1986 .

Total synthesis of oleandrose and the avermectin disaccharide, benzyl .alpha.-L-oleandrosyl-.alpha.-L-4-acetoxyoleandroside

P. G. Wuts, S. Bigelow, 1983 .

.gamma.-Alkoxyallylboronates as useful reagents for preparation of differentially protected diol derivatives

P. G. Wuts, S. Bigelow, 1982 .

3-Acyltetramic acid antibiotics. 1. Synthesis of tirandamycic acid

B. Ernst, P. G. Wuts, R. Ireland, 1981 .

Protection for the Alkyne –CH

Theodora W. Greene, P. G. Wuts, T. W. Greene, 2002 .

p‐Methoxybenzyl Chloride

P. D. Wilson, P. G. Wuts, M. Paduraru, 2007 .

Application of Allylboronates to the Synthesis of Carbomycin B.

P. G. Wuts, S. Bigelow, 1989 .

Chloromethyl Methyl Ether

P. G. Wuts, 2001 .

Stereochemical course of the cyclization of olefinic aldehydes

N. Andersen, S. Smith, H. Uh, 1972 .

USE OF A DELTA 1-PIPERIDINE FOR THE SYNTHESIS OF A DIFFERENTIALLY PROTECTED DIAMINE INTERMEDIATE FOR THE PREPARATION OF THE IRON SIDEROPHORE DESFERRIO XAMINE

P. G. Wuts, J. Havens, J. Cabaj, 1994 .

ALLYLBORONATE SYNTHESIS. SYNTHESIS OF A β-ALKOXY CARBANION EQUIVALENT

P. G. Wuts, P. Thompson, Gary R. Callen, 1984 .

4‐Methoxybenzyl 2,2,2‐Trichloro acetimidate

P. G. Wuts, 2001 .

3-Acyltetramic acid antibiotics. 1. Synthesis of tirandamycic acid

B. Ernst, P. G. Wuts, R. Ireland, 1981 .

Studies directed toward the synthesis of ionomycin (I): synthesis of the furanoid fragment

R. D'costa, W. Butler, P. G. Wuts, 1984 .

Stereorational total synthesis of the marine diterpene dictyolene and its C-11 epimer

J. A. Marshall, P. G. Wuts, J. Marshall, 1978 .

Development of a practical synthesis of sumanirole

M. White, P. G. Wuts, R. Gu, 2002 .

Synthesis of the cannabisativine skeleton via an intramolecular allylsilane-nitrone cycloaddition

Yong-woon Jung, P. G. Wuts, 1988 .

A novel synthesis of spironolactone. An application of the hydroformylation reaction

P. G. Wuts, A. Ritter, 1989 .

A cautionary note on the use of p-nitrobenzenesulfonamides as protecting groups

P. G. Wuts, Jill M. Northuis, 1998 .

Convenient Preparation of Optically Pure 3‐Aryloxy‐pyrrolidines

J. Schwarz, M. Stier, S. Maiti, 2008 .

Novel Riboswitch-Binding Flavin Analog That Protects Mice against Clostridium difficile Infection without Inhibiting Cecal Flora

R. Breaker, Daniel P. Walker, K. Blount, 2015, Antimicrobial Agents and Chemotherapy.

The Synthesis of Hydronaphthalenes fromm-Toluic AcidviaCyclization of Thioacetal Monosulfoxides

J. A. Marshall, P. G. Wuts, 1977 .

An Expedient Procedure for the Purification of the CuBr·CH3SCH3 Complex

P. G. Wuts, 1981 .

Synthesis of the hydroxyethylene isostere of Leu-Val

P. G. Wuts, A. Ritter, L. Pruitt, 1992 .

A new and more practical approach to the synthesis of the precursor of SC-84536, a selective inducible nitric oxide synthase inhibitor

P. G. Wuts, 2008 .

Novel Riboswitch-Binding Flavin Analog That Protects Mice against Clostridium difficile Infection without Inhibiting Cecal Flora

R. Breaker, Daniel P. Walker, C. Megyola, 2015, Antimicrobial Agents and Chemotherapy.

Benzothiazole‐2‐sulfonyl Chloride

P. G. Wuts, 2005 .

A new method for deprotection of benzothiazolesulfonamides using a thiol and base

P. G. Wuts, R. Gu, Collette L. Thomas, 1998 .

Cleavage of N′,N′-Dialkylhydrazides with PhI(OH)OTs.

P. G. Wuts, M. Goble, 2000 .