Weinreb, Steven M.
Steven M. Weinreb American chemist
Weinreb, Steven M., 1941-
VIAF ID: 50285131 (Personal)
Permalink: http://viaf.org/viaf/50285131
Preferred Forms
- 100 0 _ ‡a Steven M. Weinreb ‡c American chemist
- 200 _ | ‡a Weinreb ‡b Steven M.
-
-
- 100 1 _ ‡a Weinreb, Steven M.
-
-
- 100 1 _ ‡a Weinreb, Steven M.
- 100 1 0 ‡a Weinreb, Steven M.
-
-
- 100 1 _ ‡a Weinreb, Steven M.
-
4xx's: Alternate Name Forms (20)
Works
Title | Sources |
---|---|
Acetone Oxime | |
Alkaloid total synthesis by intramolecular imino Diels-Alder cycloadditions | |
The Alstoscholarisine Alkaloids: Isolation, Structure Determination, Biogenesis, Biological Evaluation, and Synthesis | |
An Approach to the Total Synthesis of the Marine Ascidian Metabolite Perophoramidine via a Halogen-Selective Tandem Heck/Carbonylation Strategy | |
Construction of beta-haloenamides via direct copper-promoted coupling of lactams with 2-chloro and 2-bromo vinyliodides. | |
Construction of the azocane (azacyclooctane) moiety of the Lycopodium alkaloid lycopladine H via an intramolecular hydroaminomethylation strategy. | |
Convergent approach to the tetracyclic core of the apparicine class of indole alkaloids via a key intermolecular nitrosoalkene conjugate addition | |
Diels-Alder Reactions of Imino Dienophiles | |
A direct conversion of esters to nitriles | |
Efficient methodology for alkylation of vinylnitroso compounds with carbon nucleophiles. | |
An expedient reductive method for conversion of ketoximes to the corresponding carbonyl compounds. | |
The first examples of ring-closing olefin metathesis of vinyl chlorides | |
Further studies of intramolecular Michael reactions of nitrosoalkenes for construction of functionalized bridged ring systems. | |
Hetarenes and related ring systems | |
Hetero Diels-Alder methodology in organic synthesis | |
Imino Diels-Alder-Based Construction of a Piperidine A-Ring Unit for Total Synthesis of the Marine Hepatotoxin Cylindrospermopsin | |
Lepadiformine: a case study of the value of total synthesis in natural product structure elucidation | |
A mild, convenient, and inexpensive procedure for conversion of vinyl halides to alpha-haloketones | |
A mild, efficient method for the oxidation of alpha-diazo-beta-hydroxyesters to alpha-diazo-beta-ketoesters | |
N-methoxy-n-methylamides as effective acylating agents | |
A new total synthesis of the zinc matrixmetalloproteinase inhibitor ageladine A featuring a biogenetically patterned 6pi-2-azatriene electrocyclization | |
Science of synthesis : Houben-Weyl methods of molecular transformations. | |
Six-membered hetarenes with two unlike or more than two heteroatoms and fully unsaturated larger-ring heterocycles | |
Some recent advances in the synthesis of polycyclic imidazole-containing marine natural products | |
Stereochemical investigation of conjugate additions of carbon- and heteronucleophiles to ring-substituted nitrosocyclohexenes | |
Stereoselective total syntheses and reassignment of stereochemistry of the freshwater cyanobacterial hepatotoxins cylindrospermopsin and 7-epicylindrospermopsin | |
Stereoselective total syntheses of the racemic form and the natural enantiomer of the marine alkaloid lepadiformine via a novel N-acyliminium ion/allylsilane spirocyclization strategy | |
Structures of rugulovasine-A and -B and 8-chlororugulovasine-A and -B | |
Studies of intramolecular cyclizations of N-acyliminium ions derived from acyclic ketones: unanticipated stereochemical and structural results | |
Studies on a total synthesis of the microbial immunosuppresive agent FR901483. | |
Studies on total synthesis of the cylindricine/fasicularin/lepadiformine family of tricyclic marine alkaloids | |
A study of the scope and regioselectivity of the ruthenium-catalyzed [3 + 2]-cycloaddition of azides with internal alkynes | |
Synthetic studies on perophoramidine and the communesins: construction of the vicinal quaternary stereocenters | |
tert-Butylsulfonyl (Bus), a New Protecting Group for Amines | |
Three carbon-heteroatom bonds amides and derivatives; peptides; lactams | |
Total synthesis of ageladine A, an angiogenesis inhibitor from the marine sponge Agelas nakamurai. | |
Total synthesis of the antitumor antibiotic streptonigrin | |
Total synthesis of the polycyclic fungal metabolite (+/-)-communesin F | |
Total synthesis of the tetracyclic antimalarial alkaloid (±)-myrioneurinol. | |
Total synthesis of the unusual monoterpenoid indole alkaloid (±)-alstilobanine A. | |
X-Ray structure of phlebiakauranol and phlebianorkauranol, highly oxygenated antibacterial metabolites of Phlebia strigosozonata | |
β-Tosylethylazide: a useful synthon for preparation of N-protected 1,2,3-triazoles via click chemistry | |
β-Trimethylsilylethanesulfonyl Chloride |