162.  W. R. Roush and S. Narayan, "2-Deoxy-2-Iodo-α-Mannopyranosyl and α-Talopyranosyl Acetates: Highly Stereoselective Glycosyl Donors for the Synthesis of 2-Deoxy-α-Glycosides," Org. Lett. 19991, 899. 10.1021/ol9908068

161.  W. R. Roush, S. Narayan, C. E. Bennett, and K. Briner, "Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-Iodo-α-Mannopyranosyl Acetates," Org. Lett. 19991, 895.10.1021/ol990815g

160.  W. R. Roush, B. W. Jung and C. E. Bennett, "2-Deoxy-2-Iodo and 2-Deoxy-2-Bromo-Glucopyranosyl Trichloroacetimidates: Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-Glycosides," Org. Lett. 19991, 891. 10.1021/ol9908070

159.  W. R. Roush and G. C. Lane, "Studies on the Synthesis of Tedanolide: Synthesis of the C(5)-C(21) Segment via a Highly Stereoselective Fragment Assembly Aldol Reaction of a Chiral β,γ-Unsaturated Methyl Ketone", Org. Lett.19991, 95.10.1021/ol990572s

158.  W. R. Roush and G. J. Dilley, "Studies of Fragment Assembly Aldol Reactions of Chiral Aldehydes and Chiral Methyl Ketones: Stereoselective Synthesis of the C(13)-C(25) Segment of Scytophycin C," Tetrahedron Lett.199940, 4955. 10.1016/S0040-4039(99)00868-0

157.  W. R. Roush, A. Alvarez Hernandez, and G. Zepeda, "A New Synthesis of Peptidyl Epoxysuccinates for Probing Cysteine Protease-Inhibitor P3-S3 Binding Interactions", Synthesis1999, 1500. 10.1055/s-1999-3648

156.  G. C. Micalizio and W. R. Roush, "Towards the Synthesis of Spongistatin 1: Diastereoselective Synthesis of the C(36)-C(45) Subunit", Tetrahedron Lett.199940, 3351. 10.1016/S0040-4039(99)00464-5

155.  S. R. Chemler and W. R. Roush, "Stereochemically Divergent Pathways for the Allylation and Crotylation Reactions of Anti- and Syn-β-Hydroxy-α-Methyl Aldehydes with Allyl- and Crotyltrifluorosilanes", Tetrahedron Lett.199940, 4643. 10.1016/S0040-4039(99)00730-3

154.  S. R. Chemler, D. S. Coffey, and W. R. Roush, "An Improved Synthesis of the (E,Z)-Dienoate Precursor of (+)-Damavaricin D Via a Vinylogous Horner-Wadsworth-Emmons Reaction," Tetrahedron Lett.199940, 1269. 10.1016/S0040-4039(98)02638-0

153.  W. R. Roush and C. E. Bennett, "A Highly Stereoselective Synthesis of 2-Deoxy-β-Glycosides using 2-Deoxy-2-Iodo-Glucopyranosyl Acetate Donors", J. Am. Chem. Soc.1999121, 3541. 10.1021/ja984365j

152.  W. R. Roush, R. A. Hartz and D. J. Gustin, "Total Synthesis of Olivomycin A", J. Am. Chem. Soc.1999121, 1990.10.1021/ja984229e

151.  K. A. Scheidt, A. Tasaka, T. D. Bannister, M. D. Wendt, and W. R. Roush, "Total Synthesis of (-)-Bafilomycin A1: Application of Diastereoselective Crotylboration and Methyl Ketone Aldol Reactions", Angew. Chem. Int. Ed.199938, 1652 (German version: Angew. Chem. 1999111, 1753). 10.1002/(SICI)1521-3773(19990601)38:11<1652::AID-ANIE1652>3.0.CO;2-K

150.  K. A. Scheidt, H. Chen, B. C. Follows, S. R. Chemler, D. S. Coffey, and W. R. Roush, "Tris(dimethylamino)sulfonium Difluorotrimethylsilicate (TAS-F), a Mild Reagent for the Removal of Silicon Protecting Groups," J. Org. Chem.199863, 6436.10.1021/jo981215i

149.  W. R. Roush, S. L. Gwaltney, III, J. Cheng, K. A. Scheidt, J. H. McKerrow, and E. Hansell, "Vinylsulfonates and Vinylsulfonamides: Potent, Irreversible Inhibitors of Cysteine Proteases," J. Am. Chem. Soc.1998120, 10994. 10.1021/ja981792o

148.  W. R. Roush, F. V. Gonzalez, J. H. McKerrow and E. Hansell, "Design and Synthesis of Dipeptidyl α',β'-Epoxy Ketones, Potent Irreversible Inhibitors of the Cysteine Protease Cruzain," Bioorg. Med. Chem. Lett.19988, 2809. 10.1016/S0960-894X(98)00494-6

147.  K. A. Scheidt, W. R. Roush, J. H. McKerrow, P. M. Selzer, E. Hansell, and P. J. Rosenthal, "Structure-Based Design, Synthesis and Evaluation of Conformationally Constrained Cysteine Protease Inhibitors," Bioorg. Med. Chem.19986, 2477. 10.1016/S0968-0896(98)80022-9

146.  W. R. Roush and R. J. Sciotti, "Enantioselective Total Synthesis of (-)-Chlorothricolide via the Tandem Inter- and Intramolecular Diels-Alder Reaction of a Hexaenoate Intermediate," J. Am. Chem. Soc.1998120, 7411. 10.1021/ja980611f

145.  W. R. Roush and R. J. Sciotti, "Studies on the Synthesis of Chlorothricolide: Diastereo- and Enantioselective Syntheses of Model Top Half Spirotetronate Units," J. Org. Chem.199863, 5473. 10.1021/jo980379w

144.  W. R. Roush, L. A. Pfeifer and T. G. Marron, "Studies on the Synthesis of the Mycalamides: Stereoselective Synthesis of a Model N-Glycosyl Pederamide via a Stereoselective Aldol Condensation," J. Org. Chem.199863, 2064. 10.1021/jo980023k

143.  W. R. Roush and L. A. Pfeifer, "Stereoselective N-Acylation Reactions of α-Alkoxy Carbamates," J. Org. Chem.199863, 2062.10.1021/jo980024c

142.  S. R. Chemler and W. R. Roush, "Concerning the Synthesis of the Elusive Anti, Anti-Dipropionate Stereotriad via the Crotylation of β-Hydroxy-α-Methyl Aldehydes with (Z)-Crotyltrifluorosilane. Application to the Synthesis of the C(7)-C(16) Segment of Zincophorin," J. Org. Chem.199863, 3800. 10.1021/jo980387c

141.  W. R. Roush and D. A. Barda, "Second Generation Synthesis of the Quartromycin Spirotetronic Acid Submits Via a Claisen Rearrangement-Intramolecular Aldol Sequence," Tetrahedron Lett199738, 8785. 10.1016/S0040-4039(97)10416-6

140.  W. R. Roush and D. A. Barda, "An Intramolecular Diels-Alder Approach to the Spirotetronic Acid Subunits of the Quartromicins,"Tetrahedron Lett.199738, 8781. 10.1016/S0040-4039(97)10415-4

139.  W. R. Roush , M. L. Reilly, K. Koyama and B. B. Brown, "A Formal Total Synthesis of (+)-Tetronolide, the Aglycone of the Tetrocarcins: Enantio- and Diastereoselective Syntheses of the Octahydronaphthalene (Bottom Half) and Spirotetronate (Top Half) Fragments," J. Org. Chem.199762, 8708. 10.1021/jo970960c

138.  W. R. Roush, D. S. Coffey and D. J. Madar, "Total Synthesis of Damavaricin D," J. Am. Chem Soc.1997119, 11331.10.1021/ja971828x

137.  W. R. Roush and D. A. Barda, "Highly Selective Lewis Acid Catalyzed Diels-Alder Reactions of Acyclic (Z)-1,3-Dienes," J. Am. Chem Soc.1997119, 7402. 10.1021/ja971070h

136.  W. R. Roush, D. P. Sebesta, and R. A. James, "Stereoselective Synthesis of 2-Deoxy-β-glycosides From Glycal Precursors. 2. Stereochemistry of Glycosidation Reactions of 2-Thiophenyl- and 2-Selenophenyl-α-D-gluco-pyranosyl Donors" Tetrahedron199753, 8837. 10.1016/S0040-4020(97)90395-1

135.  W. R. Roush, D. P. Sebesta, and C. E. Bennett, "Stereoselective Synthesis of 2-Deoxy-β-glycosides From Glycal Precursors. 1. Stereochemistry of the Reactions of D-Glucal Derivatives with Phenylsulfenyl Chloride and Phenylselenenyl Chloride," Tetrahedron,199753, 8825. 10.1016/S0040-4020(97)90394-X

134.  W. R. Roush and A. B. Works, "Diastereofacially Selective Enolate Claisen Rearrangements of [4-7-h4-(1-Acyloxy-2,4,6-octadienyl)]tricarbonyliron Complexes," Tetrahedron Lett199738, 351. 10.1016/S0040-4039(96)02349-0

133.  W. R. Roush, T. G. Marron, and L. A. Pfeifer, "A Highly Diastereoselective Total Synthesis of Pederic Acid Derivatives," J. Org. Chem.199762, 474. 10.1021/jo961841k

132.  J. A. Hunt and W. R. Roush, "4,5-Diisopropyl-B-[(E)-3'-(menthofuryldimethylsilyl)-allyl]-1,3,2-dioxaborolane, An Improved Chiral Reagent for the Anti α-Hydroxyallylation of Aldehydes: Application to the Enantioselective Synthesis of (-)-Swainsonine," J. Org. Chem.,199762, 1112. 10.1021/jo961840s

131.  W. R. Roush, J. A. Champoux and B. C. Peterson, "Diastereoselective Synthesis of the Cis-Octahydronaphthalene Nucleus of Superstolides A and B," Tetrahedron Lett.199637, 8989. 10.1016/S0040-4039(96)02110-7

130.  W. R. Roush and A. B. Works, "Diastereoselective Synthesis of the Trans-anti-cis-decahydro-as-Indacene Ring System via the Transannular Diels-Alder Reaction of a Functionalized (E,E,E)-Cyclododeca-1,6,8-Triene," Tetrahedron Lett.199637, 8065.10.1016/0040-4039(96)01840-0

129.  J. A. Hunt and W. R. Roush, "Solid-Phase Synthesis of 6-Deoxy-Oligosaccharides," J. Am. Chem. Soc.1996118, 9998.10.1021/ja962128f

128.  W. R. Roush, K. Briner, B. S. Kesler, M. Murphy, and D. J. Gustin, "Studies on the Synthesis of Aureolic Acid Antibiotics: Acyloin Glycosidations," J. Org. Chem. 199661, 6098. 10.1021/jo960932e

127.  W. R. Roush, D. S. Coffey, D. J. Madar and A. D. Palkowitz, "Studies on the Synthesis of the Streptovaricins: Total Synthesis of 24,27-Dimethyl Dihydrodamavaricin D," J. Brazil. Chem. Soc. 19967, 327. Read Online

126.  W. R. Roush, K. Koyama, M. L. Curtin and K. J. Moriarty, "Studies on the Synthesis of Nargenicin A1: Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels-Alder Reaction of an 18-Membered Macrolide," J. Am. Chem. Soc. 1996118, 7502. 10.1021/ja9607796

125.  W. R. Roush, "Allylaluminum Reagents," in Methods of Organic Chemistry (Houben-Weyl), 1995, Vol. E 21, p. 1487; Georg Thieme Verlag, Stuttgart.

124.  W. R. Roush, "Allylboron Reagents," in Methods of Organic Chemistry (Houben-Weyl), 1995, Vol. E 21, p. 1410; Georg Thieme Verlag, Stuttgart.

123.  W. R. Roush and P. T. Grover, "N,N'-Bis-(2,2,2-trifluoroethyl)-N,N'-ethylene Tartramide: An Improved Chiral Auxiliary for the Asymmetric Allylboration Reaction," J. Org. Chem.199560, 3806. 10.1021/jo00117a036

122.  D. S. Coffey and W. R. Roush, "Synthesis of the Naphthoquinone Nucleus of Awamycin," J. Org. Chem.199560, 4412.10.1021/jo00119a018

121.  D. J. Gustin, M. S. VanNieuwenhze and W. R. Roush, "Synthesis of the C(3)-C(15) Segment of Rutamycin B via a C(8)-C(9) Fragment Assemble Aldol Reaction: Metal Dependence of the Aldehyde and Enolate Diastereofacial Selectivities," Tetrahedron Lett.,199536, 3447. 10.1016/0040-4039(95)00628-P

120.  D. J. Gustin, M. S. VanNieuwenhze and W. R. Roush, "Diastereoselective Aldol Reactions of Chiral Aldehydes and Chiral Methyl Ketones: Dependence of Stereoselectivity on the Metal Enolate, the Aldehyde 2,3-Stereochemistry, and the β-Alkoxy Protecting Group of the Chiral Aldehyde," Tetrahedron Lett.199536, 3443. 10.1016/0040-4039(95)00626-N

119.  W. R. Roush and X.-F. Lin, "Studies on the Synthesis of Aureolic Acid Antibiotics: Highly Stereoselective Synthesis of Aryl 2-Deoxy-β-glycosides via the Mitsunobu Reaction and Synthesis of the Olivomycin A-B Disaccharide," J. Am. Chem. Soc.1995117, 2236.10.1021/ja00113a013

118.  J. A. Hunt and W. R. Roush, "Diisopropyl Tartrate-Modified (E)-γ-[(Menthofuryl)dimethyl-silyl]allylboronate, an Improved Chiral Reagent for the Anti α-Hydroxyallylation of Aldehydes. Application to the Enantioselective Synthesis of (-)-Swainsonine," Tetrahedron Lett. 199536, 501. 10.1016/0040-4039(94)02295-M

117.  W. R. Roush and J. A. Hunt, "Asymmetric Allylboration of 2(N),3(O)-Isopropylidene-N-Boc-L-Serinal: Diastereoselective Synthesis of the Calicheamicin γ1I Amino Sugar," J. Org. Chem.199560, 798. 10.1021/jo00109a008

116.  T. G. Marron and W. R. Roush, "Diastereoselective Synthesis of N-Benzoyl Mycalamine, the Fully Elaborated Trioxadecalin Nucleus of Mycalamide A. Control of the Key N-Acyl Aminal Stereocenter via Carbamate Acylation," Tetrahedron Lett.199536, 1581.10.1016/0040-4039(95)00093-R

115.  C. K. Wada and W. R. Roush, "Highly Stereoselective 1,4-Addition Reactions of Alkylidene Malonate Substituted η4-(1,3-Butadienyl)iron(tricarbonyl) Complexes," Tetrahedron Lett. 199435, 7351. 10.1016/0040-4039(94)85311-8

114.  W. R. Roush and C. K. Wada, "Highly Stereoselective Substitution Reactions of Functionalized η4-[3(E),5(E)-Heptadien-2-ol]iron Tricarbonyl Complexes," Tetrahedron Lett. 199435, 7347. 10.1016/0040-4039(94)85310-X

113.  M. S. VanNieuwenhze and W. R. Roush, "(Z)-γ-[(Diisopropylidene-α-D-mannopyranosyl)-oxy]allyltributylstannane: A New Chiral Reagent for the Asymmetric α-Hydroxyallylation of Aldehydes," J. Am. Chem. Soc. 1994116, 8536. 10.1021/ja00098a014

112.  W. R. Roush and B. C. Follows, "Asymmetric Synthesis of the Hydroxylamino Sugar of Calicheamicin," Tetrahedron Lett. 199435, 4935. 10.1016/S0040-4039(00)73286-2

111.  W. R. Roush and D. J. Gustin, "A Stereochemically General Synthesis of Methyl 2,4,6-Trideoxy-4-methylthio-α-D-ribo-hexopyranoside, the Thio Sugar of Esperamicin A1," Tetrahedron Lett. 199435, 4931. 10.1016/S0040-4039(00)73285-0

110.  W. R. Roush and R. J. Sciotti, "Enantioselective Total Synthesis of (-)-Chlorothricolide," J. Am. Chem. Soc. 1994116, 6457.10.1021/ja00093a065

109.  Z. Li, X. Chen, E. Davidson, O. Zwang, C. Mendis, C. S. Ring, W. R. Roush, G. Fegley, R. Li, P. J. Rosenthal, G. Lee, G. L. Kenyon, I. D. Kuntz and F. E. Cohen, "A Structure-Based Approach to Malaria Chemotherapy," Chemistry & Biology19941, 31. 10.1016/1074-5521(94)90038-8

108.  W. R. Roush, P. T. Grover and T. G. Marron, "Allylboronates in Organic Synthesis: Design of an Improved Chiral Auxiliary and Synthesis of the Trioxadecalin Nucleus of Mycalamides A and B," in "Current Topics in the Chemistry of Boron," G. W. Kabalka, ed., Royal Society of Chemistry, 1994, 113.

107.  W. R. Roush and C. K. Wada, "Application of η4-Diene Iron Tricarbonyl Complexes in Acyclic Stereocontrol: Asymmetric Synthesis of the as-Indacene Unit of Ikarugamycin (A Formal Total Synthesis)," J. Am. Chem. Soc. 1994116, 2151. 10.1021/ja00084a068

106.  W. R. Roush, T. D. Bannister, and M. D. Wendt, "Concerning the Diastereofacial Selectivity of Aldol Reactions of Chiral Methyl Ketone Enolates: Evidence for Remote Chelation in the Bafilomycin Aldol Reaction," Tetrahedron Lett. 199334, 8387. 

105.  W. R. Roush and X. F. Lin, "Synthesis of Naphthyl A-B Disaccharides Corresponding to Olivomycin A and Mithramycin,"Tetrahedron Lett. 199334, 6829. 10.1016/S0040-4039(00)91806-9

104.  W. R. Roush and T. G. Marron, "Towards the Synthesis of Mycalamides A, B, and Onnamide A: A Highly Stereoselective Synthesis of the Trioxadecalin Ring System," Tetrahedron Lett.1993 34, 5421. 10.1016/S0040-4039(00)73924-4

103.  W. R. Roush, J. S. Warmus, and A. B. Works, "Synthesis and Transannular Diels-Alder Reactions of (E,E,E)-Cyclotetradeca-2,8,10-trienones," Tetrahedron Lett. 199334, 4427. 10.1016/0040-4039(93)88050-S

102.  W. R. Roush, K. Briner and D. P. Sebesta, "Highly Stereoselective Synthesis of α-L-Olivomycosides via Trimethylsilyl Triflate Mediated Glycosidations of 1-O-Acetyl-4-O-isobutyryl-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranose," SynLett 1993, 264.10.1055/s-1993-22425

101.  W. R. Roush and D. J. Madar, "Towards the Synthesis of Streptovaricin D: Synthesis of Fully Elaborated Aromatic Precursors and Coupling with Ansa Chain Fragments," Tetrahedron Lett. 199334, 1553. 10.1016/0040-4039(93)85004-G

100.  W. R. Roush and B. B. Brown, "Studies on the Synthesis of Kijanolide: Synthesis of the 2-Acyl Spiro Tetronate and Investigations Concerning the Coupling of the Top and Bottom Half Fragments," J. Org. Chem. 199358, 2162. 10.1021/jo00060a036

99.  W. R. Roush and B. B. Brown, "A Highly Diastereo- and Enantioselective Synthesis of the Top Half of Kijanolide," J. Org. Chem.199358, 2151. 10.1021/jo00060a035

98.  W. R. Roush and B. B. Brown, "Application of the Steric Directing Group Strategy to the Stereoselective Synthesis of the Octahydronaphthalene Substructure of Kijanolide and Tetronolide," J. Am. Chem. Soc. 1993115, 2268. 10.1021/ja00059a024

97.  W. R. Roush and K. Koyama, "Enantioselective Synthesis of the Top Half of Tetronolide," Tetrahedron Lett. 199233, 6227.10.1016/S0040-4039(00)60939-5

96.  W. R. Roush and M. Murphy, "An Improved Synthesis of Naphthoate Precursors to Olivin", J. Org. Chem. 199257, 6622.10.1021/jo00050a047

95.  D. P. Sebesta and W. R. Roush, "Synthesis of CDE Trisaccharide Precursors of Olivomycin A," J. Org. Chem. 199257, 4799.10.1021/jo00044a010

94.  W. R. Roush and R. J. Sciotti, "Enantioselective Synthesis of the Top Half of Chlorothricolide," Tetrahedron Lett. 199233, 4691.10.1016/S0040-4039(00)61260-1

93.  W. R. Roush and T. D. Bannister, "Stereoselective Synthesis of the C(13)-C(25) Segment of Bafilomycin A1," Tetrahedron Lett.199233, 3587. 10.1016/S0040-4039(00)92509-7

92.  W. R. Roush and B. B. Brown, "Enantioselective Synthesis of 2-Alkyl-5-methylene-1,3-dioxolan-4-ones and Exo-Selective Diels-Alder Reactions with Cyclopentadiene," J. Org. Chem. 199257, 3380. 10.1021/jo00038a028

91.  W. R. Roush, A. M. Ratz, and J. A. Jablonowski, "Solid State and Solution Conformational Analysis of Tartrate Derived 1,3-Dioxolanes and 1,3,2-Dioxaborolanes," J. Org. Chem. 199257, 2047. 10.1021/jo00033a027

90.  W. R. Roush and P. T. Grover, "Diisopropyl Tartrate Modified (E)-γ-[(Cyclohexyloxy)-dimethylsilyl]- and (E)-γ-(Dimethylphenylsilyl)allylboronates: Chiral Reagents for the Enantio- and Diastereoselective Synthesis of Anti 1,2-Diols and 2-Butene-1,4-diols via the Formal α- and γ-Hydroxyallylation of Aldehydes," Tetrahedron 199248, 1981. 10.1016/S0040-4020(01)88869-4

89.  W. R. Roush and J. C. Park, "Asymmetric Allylborations of 3-Decynal Dicobalt Hexacarbonyl: Cobalt Induced Reversal of Enantioselectivity and Applications to Highly Diastereoselective Intramolecular Pauson-Khand Reactions," Tetrahedron Lett. 199132, 6285. 10.1016/0040-4039(91)80148-Y

88.  W. R. Roush and X.-F. Lin, "A Highly Stereoselective Synthesis of Aryl 2-Deoxy-β-glycosides via the Mitsunobu Reaction," J. Org. Chem. 199156, 5740. 10.1021/jo00020a003

87.  W. R. Roush and P. T. Grover, "Diisopropyl Tartrate (E)-γ-(Dimethylphenylsilyl)-Allylboronate, a Chiral Allylic Alcohol β-Carbanion Equivalent for the Enantioselective Synthesis of 2-Butene-1,4-diols from Aldehydes," Tetrahedron Lett. 199031, 7567. 10.1016/S0040-4039(00)97300-3

86.  W. R. Roush, P. T. Grover, and X. Lin, "Diisopropyl Tartrate Modified (E)-γ-[(Cyclohexyl-oxy)dimethyl)silyl]Allylboronate, a Chiral Reagent for the Stereoselective Synthesis of Anti 1,2-Diols via the Formal α-Hydroxyallylation of Aldehydes," Tetrahedron Lett. 199031, 7563. 10.1016/S0040-4039(00)97299-X

85.  W. R. Roush, "Concerning the Diastereofacial Selectivity of Aldol Reactions of α-Methyl Chiral Aldehydes and Lithium and Boron Propionate Enolates" J. Org. Chem. 199156, 4151. 10.1021/jo00013a015

84. 84. W. R. Roush, K. J. Moriarty, and B. B. Brown, "Stereoselective Synthesis of (Z,E)-2-Bromo-1,3-dienes via the Palladium (0) Catalyzed Cross Coupling Reactions of 1,1-Dibromoolefins and Vinylboronic Acids," Tetrahedron Lett. 1990, 31, 6509. 10.1016/S0040-4039(00)97103-X

83.  W. R. Roush, M. Kageyama, R. Riva, B. B. Brown, J. S. Warmus, and K. J. Moriarty, "Enantioselective Synthesis of the Bottom Half of Chlorothricolide. 3. Studies of the Steric Directing Group Strategy for Stereocontrol in Intramolecular Diels-Alder Reactions," J. Org. Chem. 199156, 1192. 10.1021/jo00003a049

82.  W. R. Roush and J. C. Park, "Asymmetric Allylborations of Diene Aldehyde Fe(CO)3 Derivatives: Efficient Kinetic Resolution of Racemic Complexes and the Highly Enantiotopic Group and Face Selective Allylboration of a Meso Substrate," Tetrahedron Lett. 1990,31, 4707. 10.1016/S0040-4039(00)97712-8

81.  W. R. Roush, X. Lin, and J. A. Straub, "A Highly Stereoselective Synthesis of the AB Disaccharide Unit of Olivomycin A", J. Org. Chem. 199156, 1649. 10.1021/jo00004a054

80.  W. R. Roush, J. A. Straub, and M. S. VanNieuwenhze, "A Stereochemically General Synthesis of 2-Deoxyhexoses via the Asymmetric Allylboration of 2,3-Epoxyaldehydes," J. Org. Chem. 199156, 1636. 10.1021/jo00004a053

79. 79. W. R. Roush, A. D. Palkowitz, and K. A. Ando, "Acyclic Diastereoselective Synthesis Using Tartrate Ester Modified Crotylboronates. Double Asymmetric Reactions with α-Methyl Chiral Aldehydes and Synthesis of the C(19)-C(29) Segment of Rifamycin S," J. Am. Chem. Soc. 1990, 112, 6348. 10.1021/ja00173a024

78.  W. R. Roush, K. Ando, D. B. Powers, A. D. Palkowitz, and R. L. Halterman, "Asymmetric Synthesis Using Diisopropyl Tartrate Modified (E)- and (Z)-Crotylboronates: Preparation of the Chiral Crotylboronates and Reactions with Achiral Aldehydes," J. Am. Chem. Soc. 1990112, 6339. 10.1021/ja00173a023

77.  W. R. Roush, L. K. Hoong, M. A. J. Palmer, J. A. Straub, and A. D. Palkowitz, "Asymmetric Synthesis Using Tartrate Ester Modified Allylboronates. 2. Single and Double Asymmetric Reactions with Alkoxy-Substituted Aldehydes," J. Org. Chem. 199055, 4117.10.1021/jo00300a032

76.  W. R. Roush, L. K. Hoong, M. A. J. Palmer and J. C. Park, "Asymmetric Synthesis Using Tartrate Ester Modified Allylboronates. 1. Factors Influencing Stereoselectivity," J. Org. Chem. 199055, 4109. 10.1021/jo00300a031

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