Studies in polypropionate synthesis: High π-face selectivity in syn and anti aldol reactions of chiral boron enolates of lactate-derived ketones
Tetrahedron Letters
(1994)
35
9083
(doi: 10.1016/0040-4039(94)88434-X)
Manipulation of the aldol adducts from lactate-derived ketones. A versatile chiral auxiliary for the asymmetric synthesis of β-hydroxy carbonyl compounds
Tetrahedron Letters
(1994)
35
9087
(doi: 10.1016/0040-4039(94)88435-8)
A configurational model for siphonariid polypropionates derived from structural and biosynthetic considerations
Tetrahedron Letters
(1994)
35
{6929-6932}
(doi: 10.1016/0040-4039(94)85044-5)
Assignment of the absolute configuration of the siphonarins and baconipyrones. Enantiocontrolled synthesis of a γ-pyrone subunit
Tetrahedron Letters
(1994)
35
6925
(doi: 10.1016/0040-4039(94)85043-7)
Towards the synthesis of swinholide A and scytophycin C. A highly stereocontrolled synthesis of (−)-pre-swinholide A
Tetrahedron Letters
(1994)
35
3405
Computer-assisted design of chiral boron enolates: The role of ate complexes in determining aldol stereoselectivity.
Tetrahedron
(1994)
50
1227
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
{1711-1718}
(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
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)
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)
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
The Rational Design of Highly Stereoselective Boron Enolates Using Transition-State Computer Modeling: A Novel, Asymmetric Anti Aldol Reaction for Ketones
The Journal of Organic Chemistry
(1992)
57
5173
(doi: 10.1021/jo00045a033)
