Computer-assisted design of chiral boron enolates: The role of ate complexes in determining aldol stereoselectivity.
Tetrahedron
(1994)
50
{1227-1242}
Studies in marine macrolide synthesis: Boron and silicon-mediated coupling strategies for Swinholide A
Tetrahedron Letters
(1994)
35
441
(doi: 10.1016/0040-4039(94)85075-5)
Recent developments in asymmetric aldol methodology
Contemporary Organic Synthesis
(1994)
1
317
Studies in biomimetic polyether synthesis: Construction of an ABCD-ring subunit of etheromycin using polyepoxide cascade cyclisations.
Tetrahedron Letters
(1993)
34
7137
Studies in marine macrolide synthesis: Asymmetric synthesis of C1-C15/C16 subunits of swinholide A and scytophycin C.
Tetrahedron Letters
(1993)
34
5351
Studies in marine macrolide synthesis: A stereocontrolled synthesis of a C17-C32 subunit of scytophycin C.
Tetrahedron Letters
(1993)
34
5347
1,3-ASYMMETRIC INDUCTION IN THE ALDOL REACTIONS OF ALPHA-METHYLENE-BETA-ALKOXY ALDEHYDES
Tetrahedron Letters
(1993)
34
4393
Studies in biomimetic polyether synthesis: Synthesis of an A-ring subunit of etheromycin
Tetrahedron Letters
(1993)
34
4389
Origins of Stereoselectivity in the Addition of Chiral Allyl- and Crotylboranes to Aldehydes: The Development and Application of a Force Field Model of the Transition State
Journal of Organic Chemistry
(1993)
58
1711
(doi: 10.1021/jo00059a019)
Origins of π-face selectivity in the aldol reactions of chiral E-enol borinates: a computational study using transition state modelling.
Tetrahedron
(1993)
49
{685-696}
The Horner-Wadsworth-Emmons Reaction in Natural Products Synthesis: Expedient Construction of Complex (E)-Enones Using Barium Hydroxide
Synlett
(1993)
1993
774
(doi: 10.1055/s-1993-22605)
Studies towards the total synthesis of the marine-derived immunosuppressant discodermolide; asymmetric synthesis of a C1–C8δ-lactone subunit
Chemical Communications
(1993)
1790
(doi: 10.1039/c39930001790)
New methods and strategies for the stereocontrolled synthesis of polypropionate-derived natural products
Pure and Applied Chemistry
(1992)
64
1821
(doi: 10.1351/pac199264121821)
Enolisation of ketones by dialkylboron chlorides and trifiates: A model for the effect of reagent leaving group substrate structure and amine base.
Tetrahedron Letters
(1992)
33
{7223-7226}
The Rational Design of Highly Stereoselective Boron Enolates Using Transition-State Computer Modeling: A Novel, Asymmetric Anti Aldol Reaction for Ketones
Journal of Organic Chemistry
(1992)
57
5173
(doi: 10.1021/jo00045a033)
meso Epoxides in Asymmetric Synthesis: Enantioselective Opening by Nucleophiles in the Presence of Chiral Lewis Acids
Angewandte Chemie International Edition in English
(1992)
31
1179
(doi: 10.1002/anie.199211791)
STUDIES IN POLYPROPIONATE SYNTHESIS - HIGH PI-FACE SELECTIVITY IN SYN ALDOL REACTIONS OF TIN(II) ENOLATES FROM (R)-1-BENZYLOXY-2-METHYLPENTAN-3-ONE AND (S)-1-BENZYLOXY-2-METHYLPENTAN-3-ONE
Tetrahedron Letters
(1992)
33
4233
Diastereofacial selectivity in the aldol reactions of chiral α-methyl aldehydes: a computer modelling approach.
Tetrahedron
(1992)
48
4439
Developing a force field for the transition state of the aldol reaction of enolborinates: Evaluation of the use of fixed point charges.
Tetrahedron
(1992)
48
4183
A stereocontrolled synthesis of a C19-C32 / C17-C30 Segment for swinholide A and misakinolide A, Cytotoxic dimeric macrolides from theonella swinhoei.
Tetrahedron Letters
(1992)
33
2847
