Larry E. Overman American chemist
Overman, Larry E., 1943-
Overman, Larry E.
Overman, Larry E., 19..-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 44534367 (Personal)
Permalink: http://viaf.org/viaf/44534367
Preferred Forms
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100 0 _
‡a
Larry E. Overman
‡c
American chemist
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200 _ |
‡a
Overman
‡b
Larry E.
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100 1 _
‡a
Overman, Larry E.
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100 1 _ ‡a Overman, Larry E.
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100 1 _
‡a
Overman, Larry E.
‡d
1943-
-
100 1 _
‡a
Overman, Larry E.,
‡d
19..-....
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100 1 _
‡a
Overman, Larry E.,
‡d
1943-
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100 1 _ ‡a Overman, Larry E., ‡d 1943-
4xx's: Alternate Name Forms (20)
5xx's: Related Names (2)
Works
| Title | Sources |
|---|---|
| Catalytic asymmetric synthesis of quaternary carbons bearing two aryl substituents. Enantioselective synthesis of 3-alkyl-3-aryl oxindoles by catalytic asymmetric intramolecular heck reactions |
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| Constructing Quaternary Carbons from N-(Acyloxy)phthalimide Precursors of Tertiary Radicals Using Visible-Light Photocatalysis |
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| Constructing quaternary stereogenic centers using tertiary organocuprates and tertiary radicals. Total synthesis of trans-clerodane natural products |
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| Construction of epidithiodioxopiperazines by directed oxidation of hydroxyproline-derived dioxopiperazines |
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| Construction of substituted cyclohexanones by reductive cyclization of 7-oxo-2,8-alkadienyl esters |
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| Designing synthetic methods and natural products synthesis, 2024: |
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| Diastereoselective Coupling of Chiral Acetonide Trisubstituted Radicals with Alkenes. |
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| Diastereoselective lithiation of (eta6-arene)dicarbonyltriphenylphosphane chromium(0) oxazoline complexes--direct preparation of enantiopure complexes having planar chiral fragments of either configuration. |
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| Direct construction of quaternary carbons from tertiary alcohols via photoredox-catalyzed fragmentation of tert-alkyl N-phthalimidoyl oxalates |
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| Divergent synthesis and chemical reactivity of bicyclic lactone fragments of complex rearranged spongian diterpenes |
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| Enantioselective Construction of Vicinal Stereogenic Quaternary Centers by Dialkylation: Practical Total Syntheses of (+)- and meso-Chimonanthine. |
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| Enantioselective syntheses of authentic sclerophytin A, sclerophytin B, and cladiell-11-ene-3,6,7-triol |
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| Evolution of a strategy for the synthesis of structurally complex batzelladine alkaloids. Enantioselective total synthesis of the proposed structure of batzelladine F and structural revision |
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| Facile Preparation of Spirolactones by an Alkoxycarbonyl Radical Cyclization-Cross-Coupling Cascade |
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| Forging C(sp)-C(sp) Bonds with Carbon-Centered Radicals in the Synthesis of Complex Molecules |
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| Forming tertiary organolithiums and organocuprates from nitrile precursors and their bimolecular reactions with carbon electrophiles to form quaternary carbon stereocenters |
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| General approach for preparing epidithiodioxopiperazines from trioxopiperazine precursors: enantioselective total syntheses of (+)- and (-)-gliocladine C, (+)-leptosin D, (+)-T988C, (+)-bionectin A, and (+)-gliocladin A. |
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| Guanidine alkaloid analogs as inhibitors of HIV-1 Nef interactions with p53, actin, and p56lck. |
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| H3K9me3 Inhibition Improves Memory, Promotes Spine Formation, and Increases BDNF Levels in the Aged Hippocampus |
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| Identification of an Unexpected 2-Oxonia[3,3]sigmatropic Rearrangement/Aldol Pathway in the Formation of Oxacyclic Rings. Total Synthesis of (+)-Aspergillin PZ. |
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| Inhibition of HIV-1 envelope-mediated fusion by synthetic batzelladine analogues. |
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| The insulin secretory action of novel polycyclic guanidines: discovery through open innovation phenotypic screening, and exploration of structure-activity relationships |
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| Metal sites in proteins and models phospatases, Lewis acids and vanadium |
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| Molecular rearrangements in the construction of complex molecules |
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| Monomeric cobalt oxazoline palladacycles (COP). Useful catalysts for catalytic asymmetric rearrangement of allylic trichloroacetimidates |
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| A new asymmetric synthesis of trans-hydroisoquinolones |
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| New cationic olefin cyclization-pinacol reactions. Ring-expanding cyclopentane annulations that directly install useful functionality in the cyclopentane ring |
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| Origins of stereoselectivities of dihydroxylations of cis-bicyclo[3.3.0]octenes |
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| Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling |
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| Palladium(II)-catalyzed enantioselective synthesis of 2-vinyl oxygen heterocycles |
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| Preparation of alpha-sulfenyl enones by thermal fragmentation of beta-sulfenyl enol triflates |
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| Pumiliotoxin alkaloids: a new class of sodium channel agents. |
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| Scope and facial selectivity of the Prins-pinacol synthesis of attached rings. |
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| Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions. |
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| Stereocontrolled synthesis of angularly substituted 1-azabicyclic rings by cationic 2-aza-cope rearrangements |
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| Stereocontrolled synthesis of triazacyclopenta[cd]pentalenes by intramolecular 1,3-dipolar cycloaddition reactions of azomethine imines. |
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| Synthesis and anticancer activity of side chain analogs of the crambescidin alkaloids. |
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| Synthesis of 2,5-Diaryl-1,5-dienes from Allylic Bromides Using Visible-Light Photoredox Catalysis |
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| Synthesis of all low-energy stereoisomers of the tris(pyrrolidinoindoline) alkaloid hodgkinsine and preliminary assessment of their antinociceptive activity |
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| Synthesis of polycyclic guanidines by cyclocondensation reactions of N-amidinyliminium ions |
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| Terminating Catalytic Asymmetric Heck Cyclizations by Stereoselective Intramolecular Capture of η-Allylpalladium Intermediates: Total Synthesis of (-)-Spirotryprostatin B and Three Stereoisomers |
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| Thwarting beta-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction This research was supported by the National Institutes of Health (grant GM-12389). M.O. thanks the Deutsche Forschungsgemein |
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| Total synthesis of (+/-)-didehydrostemofoline (asparagamine A) and (+/-)-isodidehydrostemofoline |
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| Total synthesis of (+)-sieboldine a: evolution of a pinacol-terminated cyclization strategy. |
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| Total Synthesis of (-)-Chromodorolide B By a Computationally-Guided Radical Addition/Cyclization/Fragmentation Cascade. |
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| Total synthesis of (-)-crambidine and definition of the relative configuration of its unique tetracyclic guanidinium core. |
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| Total synthesis of the reputed structure of alcyonin and reassignment of its structure |
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| Toward an enantioselective total synthesis of sarain A: construction of an advanced intermediate and rearrangement of the sarain A core under mild conditions |
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| Tricyclic Analogues of Epidithiodioxopiperazine Alkaloids with Promising In Vitro and In Vivo Antitumor Activity |
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| Tuning Stereoselection in Tethered Biginelli Condensations. Synthesis of cis- or trans-1-Oxo- and 1-Iminohexahydropyrrolo[1,2-c]pyrimidines |
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| Use of the intramolecular Heck reaction for forming congested quaternary carbon stereocenters. Stereocontrolled total synthesis of (+/-)-gelsemine. |
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| Versatile Construction of 6-Substituted cis-2,8-Dioxabicyclo[3.3.0]octan-3-ones: Short Enantioselective Total Syntheses of Cheloviolenes A and B and Dendrillolide C. |
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| A versatile synthesis of unsymmetrical 3,3'-bioxindoles: stereoselective Mukaiyama aldol reactions of 2-siloxyindoles with isatins. |
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