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Michael J. Fall
Observed name:
M. J. FALL
Institutions:
National Institute on Drug Abuse,
Eli Lilly (United States),
RTI International
Observed institutions:
National Institute on Drug Abuse,
State University of New York,
Eli Lilly (United States),
RTI International,
Wake Forest University,
University at Buffalo, State University of New York
show all 6
OpenAlex ID:
A5068435772
Asymmetric Cyclopropanations by Rhodium(II) N -(Arylsulfonyl)prolinate Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Alkenes. Practical Enantioselective Synthesis of the Four Stereoisomers of 2-Phenylcyclopropan-1-amino Acid
1996
·
Huw M. L. Davies
, Paul R. Bruzinski
, et al.
·
Journal of the American Chemical Society
·
471
Effect of diazoalkane structure on the stereoselectivity of rhodium(II) (S)-N-(arylsulfonyl)prolinate catalyzed cyclopropanations
1996
·
Huw M.L. Davies
, Paul R. Bruzinski
, et al.
·
Tetrahedron Letters
·
134
Identification of an Opioid κ Receptor Subtype-Selective N-Substituent for (+)-(3 R ,4 R )-Dimethyl-4-(3-hydroxyphenyl)piperidine
1998
·
James B. Thomas
, Michael J. Fall
, et al.
·
Journal of Medicinal Chemistry
·
53
Rapid in-plate generation of benzimidazole libraries and amide formation using EEDQ
1997
·
James B. Thomas
, Michael J. Fall
, et al.
·
Tetrahedron Letters
·
36
ChemInform Abstract: Rapid In‐Plate Generation of Benzimidazole Libraries and Amide Formation Using EEDQ.
1997
·
J. B. THOMAS
, M. J. FALL
, et al.
·
ChemInform
ChemInform Abstract: Asymmetric Cyclopropanations by Rhodium(II) N‐(Arylsulfonyl)prolinate Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Alkenes. Practical Enantioselective Synthesis of the Four Stereoisomers of 2‐Phenylcyclopropan‐1‐amino Acid.
1996
·
H. M. L. DAVIES
, P. R. BRUZINSKI
, et al.
·
ChemInform
ChemInform Abstract: Effect of the Diazoalkane Structure on the Stereoselectivity of Rhodium(II) (S)‐N‐(Arylsulfonyl)prolinate Catalyzed Cyclopropanations.
1996
·
H. M. L. DAVIES
, P. R. BRUZINSKI
, et al.
·
ChemInform
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Works count:
7
Citation count:
694
H-index:
4
I10-index:
4
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