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Currently displaying 22541 - 22560 of 30389 publications

Electronic structure and chemical potentials of molecules in spc/e water.

RM Lynden-Bell, S Murdock

ABSTR PAP AM CHEM S

(2002)

224

U501

Effective chemical information.

JM Goodman

ABSTR PAP AM CHEM S

(2002)

224

{106-CINF}

¹⁷O NMR studies of oxide-ion mobility and local order.

CP Grey, N Kim

ABSTR PAP AM CHEM S

(2002)

224

{243-INOR}

Synthesis and antitumor activity of analogs of the novel microtubule stabilizing agent discodermolide.

FR Kinder, KW Bair, WC Chen, G Florence, C Francavilla, P Geng, S Gunasekera, PT Lassota, RE Longley, MG Palermo, I Paterson, S Pomponi, TM Ramsey, L Rogers, M Sabio, N Sereinig, E Sorensen, RM Wang, A Wright, Q Guo

ABSTR PAP AM CHEM S

(2002)

224

U47

Total synthesis of Argyrin B.

SV Ley, A Priour

ABSTR PAP AM CHEM S

(2002)

224

U242

Synthetic studies toward the total synthesis of Azadirachtin.

SV Ley, BL Gray, T Durand-Reville, LB Gobbi

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U242

Application of analytical constructs to the development of an indole safety-catch linker family for solid phase organic synthesis.

JJ Scicinski, MS Congreve, SV Ley

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U175

Simulation studies of solvation in imidazolium ionic liquids.

RM Lynden-Bell, C Hanke

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U619

Synthesis of spongistatin 1 (aplyronine A) and structural analogs.

I Paterson

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U48

Fundamental aspects of heterogeneous enantioselective catalysis: Surface chemistry of methyl pyruvate and (S)-1-(1-naphthyl)ethylamine on Pt{111}.

FJ Williams, JM Bonello, RM Lambert

ABSTR PAP AM CHEM S

(2002)

224

U418

In situ electrochemical control of the composition of a bimetallic catalyst: XPS and reactor studies.

FJ Williams, A Palermo, RM Lambert

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U418

A simple method for the preparation of 3-hydroxyiminodehydroquinate,The IUPAC name for 3-hydroxyiminodehydroquinate is (1S,4R,5R)-1,4,5-trihydroxy-3-(hydroxyimino)cyclohexane-1-carboxylate. a potent inhibitor of type II dehydroquinase

C Le Sann, C Abell, AD Abell

J CHEM SOC PERK T 1

(2002)

2065

(doi: 10.1039/b206066c)