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Currently displaying 22541 - 22560 of 30393 publications

The synthesis of salmeterol using solid supported reagents.

SV Ley, RN Bream

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U115

Effective chemical information.

JM Goodman

ABSTR PAP AM CHEM S

(2002)

224

U354

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

FJ Williams, A Palermo, RM Lambert

ABSTR PAP AM CHEM S

(2002)

224

U418

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

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

Synthetic studies toward the total synthesis of Azadirachtin.

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

ABSTR PAP AM CHEM S

(2002)

224

U242

Total synthesis of Argyrin B.

SV Ley, A Priour

ABSTR PAP AM CHEM S

(2002)

224

U242

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

CP Grey, N Kim

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

{243-INOR}

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

RM Lynden-Bell, S Murdock

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(2002)

224

U501

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 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

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

Journal of the Chemical Society Perkin Transactions 1

(2002)

2065

(doi: 10.1039/b206066c)