Chiral Reagents for Asymmetric Synthesis, Volume 5

Leo A. Paquette

John Wiley & Sons, 1999 - Science - 582 pages

Derived from the renowned, Encyclopedia of Reagents for Organic Synthesis (EROS), the related editors have created a new handbook which focuses on chiral reagents used in asymmetric synthesis and is designed for the chemist at the bench. This new handbook follows the same format as the Encyclopedia, including an introduction and an alphabetical arrangement of the reagents.

As chiral reagents are the key for the successful asymmetric synthesis, choosing the right reagents is essential, in this handy reference the editors give details on how to prepare, store and use the reagents as well as providing key reactions to demonstrate where reagents have been successfully used.

• Comprehensive information on 226 reagents
• Covers 64 reagents which were not included in EROS
• All information in one easy to use volume – at an affordable price 

All reagents included will be added to e-EROS – please visit the site where you can gain access to over 50,000 reactions and 3,800 of the most frequently consulted reagents.

Visit: www.interscience.wiley.com/eros

Contents

• Ely Lactale iij ſitAſſiſſilſ: 1
• Organic Synthesis Procedures Featuring Chiral: 7
• tButyl 2tButyl3methyl4oxo1imidazolidine: 9
• SAcetocarbonylcyclopentadienyltriphenyl: 21
• 1R2S1Amino23dihydro1Hinden2ol: 27
• 2Amino3methyl11diphenyl1butanol: 36
• LAspartic Acid: 42
• 1R5R2H15Benzodithiepin34Hone 15Dioxide: 48
• R2tButyl6methyl4H13dioxin4one: 51
• Benzylmethoxymethylmethylamine: 56
• NBenzyloxycarbonylLserine BLactone: 68
• 1hepta25diene2S3Sbis: 74
• 1R1R2R2R11Bicyclopentyl22diylbis: 81
• R11Bi22naphthotitanium Dichloride: 90
• 38: 103
• 56: 119
• 57: 128
• 70: 137
• R+tButyl 2pTolylsulfinylacetate: 171
• 81: 180
• Camphorylsulfonyloxaziridine: 184
• Chloromcyclopentadienyl4R trans22dimethyl: 190
• R+Cyclohexyl2anisylmethylphosphine: 197
• RR12Diamino12ditertbutylethane: 208
• 10Dicyclohexylsulfonamidoisoborneol: 214
• Dihydroquinidine Acetate: 221
• Diisopinocamphenylborane: 228
• Glycidyl Tosylate 349 cyclopenten1one Ar246triisopropylphenyl: 425
• 2S20338aßHexahydro3hydroxymethyl8a BMethyl3propiolactone: 433
• S2HydroxyNNdimethylpropanamideOO R+MethylpTolyl Sulfoxide: 439
• Monoisopinocampheylborane: 445
• NorephedrineBorane: 454
• 2S203ao40707ax233a45677aOctahydro: 462
• tLeucine tButyl Ester 375 2R4R24Pentanediol: 468
• 8Phenylmenthyl Glyoxylate: 474
• 4S5S4Methoxymethyl2methyl5phenyl2 Pseudoephedrine: 485
• Quinine: 498
• 1R5R6RSpiro44nonane16diyl: 504
• Acid Ethyl Ester: 516
• R+3pTolylsulfinylpropionic Acid 517 LTyrosine Hydrazide: 525
• RR326Diisopropoxybenzoyloxy5oxo132: 536
• 9O1256DiOisopropylideneODglucofuranosyl: 552
• Subject Index: 555
• 189: 567
• 104: 573
• 115: 579
• 245: 582
• 265: 589
• 152: 592

About the author

Leo A. Paquette is a professor in the Department of Chemistry at Ohio State University in Columbus, Ohio. He is a distinguished professor; editor and author of a wide list of Wiley publications.

Bibliographic information

• Title: Chiral Reagents for Asymmetric Synthesis, Volume 5; Chiral reagents for asymmetric synthesis, Leo A. Paquette; Handbook of Reagents for Organic Synthesis - Reagents for Silicon-mediated Organic Synthesis; Handbook of Reagents for Organic Synthesis, Anthony J. Pearson, ISBN 0471979260, 9780471979265
• Editor: Leo A. Paquette
• Edition: illustrated, reprint
• Publisher: John Wiley & Sons, 1999
• ISBN: 0470856254, 9780470856253
• Length: 582 pages
• Subjects: Science / Chemistry / Organic; Science / Chemistry / Physical & Theoretical