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}
Molecular orbital calculations on R1R2CO·H2BF complexes: Anomeric stabilisation and conformational preferences.
Tetrahedron Letters
(1992)
33
{7219-7222}
Ligand atom partial charges assignment for complementary electrostatic potentials.
Journal of Computer-Aided Molecular Design
(1992)
6
461
(doi: 10.1007/BF00130397)
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
{5173-5177}
(doi: 10.1021/jo00045a033)
Diastereofacial selectivity in the aldol reactions of chiral α-methyl aldehydes: a computer modelling approach.
Tetrahedron
(1992)
48
{4439-4458}
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
HYPERCHEM
CHEMISTRY & INDUSTRY
(1992)
572
AN UNBOUNDED SYSTEMATIC SEARCH OF CONFORMATIONAL SPACE
JOURNAL OF COMPUTATIONAL CHEMISTRY
(1991)
12
1110
(doi: 10.1002/jcc.540120908)
MODELING TRANSITION-STATES WITH FORCE-FIELDS - DEVELOPMENT OF THE BEST POSSIBLE PARAMETERS
ABSTR PAP AM CHEM S
(1991)
202
170
Origins of stereoselectivity in chiral boron enolate aldol reactions: A computational study using transition state modellings
Tetrahedron
(1991)
47
3471
Transition-State Modeling of the Aldol Reaction of Boron Enolates: A Force Field Approach
The Journal of Organic Chemistry
(1990)
55
3576
(doi: 10.1021/jo00298a038)
Enantio- and diastereoselective aldol reactions of achiral ethyl and methyl ketones with aldehydes: the use of enol diisopinocampheylborinates
Tetrahedron
(1990)
46
4663
Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate control
Tetrahedron Letters
(1989)
30
7121
Aldol reactions of methylketones using chiral boron reagents: A reversal in aldehyde enantioface selectivity
Tetrahedron Letters
(1989)
30
997
THEORETICAL-STUDIES OF ALDOL STEREOSELECTIVITY - THE DEVELOPMENT OF A FORCE-FIELD MODEL FOR ENOL BORINATES AND THE INVESTIGATION OF CHIRAL ENOLATE PI-FACE SELECTIVITY
ABSTR PAP AM CHEM S
(1988)
196
{352-ORGN}
A force field model for boron enolates
Tetrahedron Letters
(1987)
28
5209
