Year |
Citation |
Score |
2019 |
Mason JD, Weinreb SM. The Alstoscholarisine Alkaloids: Isolation, Structure Determination, Biogenesis, Biological Evaluation, and Synthesis. The Alkaloids. Chemistry and Biology. 81: 115-150. PMID 30685049 DOI: 10.1016/Bs.Alkal.2018.09.001 |
0.352 |
|
2019 |
Weinreb SM. Nitrosoalkenes: Underappreciated Reactive Intermediates for Formation of Carbon–Carbon Bonds Synlett. 30: 1855-1866. DOI: 10.1055/S-0037-1611899 |
0.538 |
|
2018 |
Mason JD, Weinreb SM. Synthesis of Alstoscholarisines A-E, Monoterpene Indole Alkaloids with Modulating Effects on Neural Stem Cells. The Journal of Organic Chemistry. PMID 29733650 DOI: 10.1021/Acs.Joc.8B00889 |
0.449 |
|
2015 |
Chauhan PS, Sacher JR, Weinreb SM. Synthesis of the tetracyclic skeleton of the Lycopodium alkaloid lycopladine H via a pivotal double hydroformylation/intramolecular reductive amination sequence. Organic Letters. 17: 806-8. PMID 25658603 DOI: 10.1021/Ol503571A |
0.755 |
|
2015 |
Nocket AJ, Feng Y, Weinreb SM. Construction of the Myrioneuron alkaloids: a total synthesis of (±)-myrioneurinol. The Journal of Organic Chemistry. 80: 1116-29. PMID 25495901 DOI: 10.1021/Jo5026404 |
0.585 |
|
2014 |
Nocket AJ, Weinreb SM. Total synthesis of the tetracyclic antimalarial alkaloid (±)-myrioneurinol. Angewandte Chemie (International Ed. in English). 53: 14162-5. PMID 25323842 DOI: 10.1002/Anie.201407810 |
0.49 |
|
2014 |
Chauhan PS, Weinreb SM. Convergent approach to the tetracyclic core of the apparicine class of indole alkaloids via a key intermolecular nitrosoalkene conjugate addition. The Journal of Organic Chemistry. 79: 6389-93. PMID 24927230 DOI: 10.1021/Jo501067U |
0.471 |
|
2014 |
Feng Y, Majireck MM, Weinreb SM. Total syntheses of the monoterpene indole alkaloids (±)-alstilobanine A and E and (±)-angustilodine. The Journal of Organic Chemistry. 79: 7-24. PMID 24319990 DOI: 10.1021/Jo402495Q |
0.803 |
|
2014 |
Sacher JR, Weinreb SM. DISCUSSION ADDENDUM for: 2‐Trimethylsilylethanesulfonyl Chloride (SES‐Cl) Organic Syntheses. 34-43. DOI: 10.1002/0471264229.Os089.03 |
0.688 |
|
2012 |
Feng Y, Majireck MM, Weinreb SM. Total synthesis of the unusual monoterpenoid indole alkaloid (±)-alstilobanine A. Angewandte Chemie (International Ed. in English). 51: 12846-9. PMID 23161740 DOI: 10.1002/Anie.201207949 |
0.805 |
|
2012 |
Sacher JR, Weinreb SM. Construction of the azocane (azacyclooctane) moiety of the Lycopodium alkaloid lycopladine H via an intramolecular hydroaminomethylation strategy. Organic Letters. 14: 2172-5. PMID 22486178 DOI: 10.1021/Ol3007277 |
0.741 |
|
2012 |
Sengupta R, Weinreb SM. A one-pot umpolung method for preparation of α-aryl nitriles from α-chloro aldoximes via organocuprate additions to transient nitrosoalkenes Synthesis (Germany). 44: 2933-2937. DOI: 10.1055/S-0032-1316984 |
0.381 |
|
2011 |
Sacher JR, Weinreb SM. Exploratory studies towards a total synthesis of the unusual bridged tetracyclic Lycopodium alkaloid lycopladine H. Tetrahedron. 67: 10203-10207. PMID 22125345 DOI: 10.1016/J.Tet.2011.04.016 |
0.768 |
|
2011 |
Sengupta R, Witek JA, Weinreb SM. Stereochemical investigation of conjugate additions of carbon- and heteronucleophiles to ring-substituted nitrosocyclohexenes. Tetrahedron. 67: 8229-8234. PMID 22125343 DOI: 10.1016/j.tet.2011.08.054 |
0.803 |
|
2011 |
Kumar P, Li P, Korboukh I, Wang TL, Yennawar H, Weinreb SM. Further studies of intramolecular Michael reactions of nitrosoalkenes for construction of functionalized bridged ring systems. The Journal of Organic Chemistry. 76: 2094-101. PMID 21361394 DOI: 10.1021/Jo1024392 |
0.826 |
|
2011 |
Witek JA, Weinreb SM. Investigation of the stereochemistry of intermolecular conjugate additions of nucleophiles to acyclic nitrosoalkenes. Organic Letters. 13: 1258-60. PMID 21294528 DOI: 10.1021/Ol2000793 |
0.816 |
|
2011 |
Chauhan PS, Majireck MM, Weinreb SM. Regioselective α-Monochlorination of N-protected-3-piperidones Heterocycles. 84: 577-585. DOI: 10.3987/Com-11-S(P)23 |
0.743 |
|
2010 |
Majireck MM, Witek JA, Weinreb SM. An expedient reductive method for conversion of ketoximes to the corresponding carbonyl compounds. Tetrahedron Letters. 51: 3555-3557. PMID 20526432 DOI: 10.1016/J.Tetlet.2010.04.131 |
0.778 |
|
2010 |
Li P, Majireck MM, Witek JA, Weinreb SM. Efficient methodology for alkylation of vinylnitroso compounds with carbon nucleophiles. Tetrahedron Letters. 51: 2032-2035. PMID 20383272 DOI: 10.1016/J.Tetlet.2010.02.050 |
0.799 |
|
2010 |
Seo JH, Liu P, Weinreb SM. Evolution of a strategy for total synthesis of the marine fungal alkaloid (+/-)-communesin F. The Journal of Organic Chemistry. 75: 2667-80. PMID 20334369 DOI: 10.1021/Jo100339K |
0.477 |
|
2010 |
Liu P, Seo JH, Weinreb SM. Total synthesis of the polycyclic fungal metabolite (+/-)-communesin F. Angewandte Chemie (International Ed. in English). 49: 2000-3. PMID 20175174 DOI: 10.1002/Anie.200906818 |
0.332 |
|
2010 |
MATZANKE N, GREGG RJ, WEINREB SM. ChemInform Abstract: Biomimetic and Synthetic Approaches to Marine Sponge Alkaloids Derived from Bis-pyridine Macrocycles Cheminform. 29: no-no. DOI: 10.1002/chin.199823247 |
0.736 |
|
2010 |
HEINTZELMAN GR, WEINREB SM, PARVEZ M. ChemInform Abstract: Imino Diels-Alder-Based Construction of a Piperidine A-Ring Unit (X) for Total Synthesis of the Marine Hepatotoxin Cylindrospermopsin (XI). Cheminform. 27: no-no. DOI: 10.1002/chin.199647228 |
0.302 |
|
2009 |
Weinreb SM. Total synthesis of the Securinega alkaloids. Natural Product Reports. 26: 758-75. PMID 19471684 DOI: 10.1039/B902265A |
0.349 |
|
2009 |
Evans MA, Sacher JR, Weinreb SM. Exploratory studies toward a total synthesis of the marine ascidian metabolite perophoramidine Tetrahedron. 65: 6712-6719. DOI: 10.1016/J.Tet.2008.10.060 |
0.778 |
|
2008 |
Li P, Majireck MM, Korboukh I, Weinreb SM. A mild, efficient method for the oxidation of alpha-diazo-beta-hydroxyesters to alpha-diazo-beta-ketoesters. Tetrahedron Letters. 49: 3162-3164. PMID 19421308 DOI: 10.1016/J.Tetlet.2008.03.011 |
0.751 |
|
2008 |
Liu P, Hong S, Weinreb SM. Total synthesis of the Securinega alkaloid (-)-secu'amamine A. Journal of the American Chemical Society. 130: 7562-3. PMID 18491903 DOI: 10.1021/Ja802700Z |
0.669 |
|
2008 |
Liu P, Hong S, Weinreb SM. ChemInform Abstract: Total Synthesis of the Securinega Alkaloid (-)-Secu′amamine A. Cheminform. 39. DOI: 10.1002/chin.200842197 |
0.601 |
|
2007 |
Weinreb SM. Some recent advances in the synthesis of polycyclic imidazole-containing marine natural products. Natural Product Reports. 24: 931-48. PMID 17898890 DOI: 10.1039/B700206H |
0.428 |
|
2007 |
Korboukh I, Kumar P, Weinreb SM. Construction of bridged and fused ring systems via intramolecular Michael reactions of vinylnitroso compounds. Journal of the American Chemical Society. 129: 10342-3. PMID 17676743 DOI: 10.1021/Ja074108R |
0.813 |
|
2007 |
Meketa ML, Weinreb SM, Nakao Y, Fusetani N. Application of a 6pi-1-azatriene electrocyclization strategy to the total synthesis of the marine sponge metabolite ageladine A and biological evaluation of synthetic analogues. The Journal of Organic Chemistry. 72: 4892-9. PMID 17539689 DOI: 10.1021/jo0707232 |
0.399 |
|
2007 |
Meketa ML, Weinreb SM. A new total synthesis of the zinc matrixmetalloproteinase inhibitor ageladine A featuring a biogenetically patterned 6pi-2-azatriene electrocyclization. Organic Letters. 9: 853-5. PMID 17261003 DOI: 10.1021/ol063038a |
0.345 |
|
2007 |
Meketa ML, Weinreb SM. A convergent total synthesis of the marine sponge alkaloid ageladine A via a strategic 6π-2-azatriene electrocyclization Tetrahedron. 63: 9112-9119. DOI: 10.1016/J.Tet.2007.06.089 |
0.442 |
|
2006 |
Seo JH, Artman GD, Weinreb SM. Synthetic studies on perophoramidine and the communesins: construction of the vicinal quaternary stereocenters. The Journal of Organic Chemistry. 71: 8891-900. PMID 17081020 DOI: 10.1021/Jo061660A |
0.805 |
|
2006 |
Majireck MM, Weinreb SM. A study of the scope and regioselectivity of the ruthenium-catalyzed [3 + 2]-cycloaddition of azides with internal alkynes. The Journal of Organic Chemistry. 71: 8680-3. PMID 17064059 DOI: 10.1021/Jo061688M |
0.815 |
|
2006 |
Weinreb SM. Studies on total synthesis of the cylindricine/fasicularin/lepadiformine family of tricyclic marine alkaloids. Chemical Reviews. 106: 2531-49. PMID 16771458 DOI: 10.1021/Cr050069V |
0.34 |
|
2006 |
Jeong JH, Weinreb SM. Formal total synthesis of the cytotoxic marine ascidian alkaloid haouamine A. Organic Letters. 8: 2309-12. PMID 16706513 DOI: 10.1021/Ol060556C |
0.616 |
|
2006 |
Sun C, Camp JE, Weinreb SM. Construction of beta-haloenamides via direct copper-promoted coupling of lactams with 2-chloro and 2-bromo vinyliodides. Organic Letters. 8: 1779-81. PMID 16623549 DOI: 10.1021/Ol060093A |
0.729 |
|
2006 |
Sun C, Lin X, Weinreb SM. Explorations on the total synthesis of the unusual marine alkaloid chartelline A. The Journal of Organic Chemistry. 71: 3159-66. PMID 16599614 DOI: 10.1021/Jo060084F |
0.722 |
|
2006 |
Meketa ML, Weinreb SM. Total synthesis of ageladine A, an angiogenesis inhibitor from the marine sponge Agelas nakamurai. Organic Letters. 8: 1443-6. PMID 16562912 DOI: 10.1021/ol0602304 |
0.371 |
|
2006 |
Hong S, Yang J, Weinreb SM. Construction of an advanced tetracyclic intermediate for total synthesis of the marine alkaloid sarain A. The Journal of Organic Chemistry. 71: 2078-89. PMID 16496996 DOI: 10.1021/Jo052504R |
0.669 |
|
2006 |
Kropf JE, Meigh IC, Bebbington MW, Weinreb SM. Studies on a total synthesis of the microbial immunosuppresive agent FR901483. The Journal of Organic Chemistry. 71: 2046-55. PMID 16496992 DOI: 10.1021/Jo052466B |
0.832 |
|
2006 |
Sun C, Weinreb SM. Preparation and allylation of enamides and enecarbamates generated via iron(0) reduction of oximes and derivatives Synthesis. 3585-3588. DOI: 10.1055/S-2006-942513 |
0.55 |
|
2006 |
Chao W, Mahajan YR, Weinreb SM. An approach to total synthesis of the cylindricine B pyridoquinoline subclass of tricyclic marine ascidian alkaloids Tetrahedron Letters. 47: 3815-3818. DOI: 10.1016/J.Tetlet.2006.03.195 |
0.652 |
|
2006 |
Heintzelman GR, Meigh IR, Mahajan YR, Weinreb SM. Diels—Alder Reactions of Imino Dienophiles Cheminform. 37. DOI: 10.1002/0471264180.Or065.02 |
0.446 |
|
2005 |
Meketa ML, Mahajan YR, Weinreb SM. An efficacious method for the halogenation of β-dicarbonyl compounds under mildly acidic conditions Tetrahedron Letters. 46: 4749-4751. DOI: 10.1016/J.Tetlet.2005.05.055 |
0.336 |
|
2004 |
Chao W, Meketa ML, Weinreb SM. Ring-closing metathesis of vinyl chlorides for formation of 5-, 6- and 7-membered carbocyclic and heterocyclic systems Synthesis. 2058-2061. DOI: 10.1055/S-2004-822327 |
0.655 |
|
2004 |
Dastrup DM, Yap AH, Weinreb SM, Henry JR, Lechleiter AJ. Synthesis of β-tosylethylhydrazine and its use in preparation of N-protected pyrazoles and 5-aminopyrazoles Tetrahedron. 60: 901-906. DOI: 10.1016/J.Tet.2003.11.046 |
0.382 |
|
2003 |
Chao W, Waldman JH, Weinreb SM. Studies of intramolecular cyclizations of N-acyliminium ions derived from acyclic ketones: unanticipated stereochemical and structural results. Organic Letters. 5: 2915-8. PMID 12889907 DOI: 10.1021/Ol035046M |
0.632 |
|
2003 |
Chao W, Weinreb SM. The first examples of ring-closing olefin metathesis of vinyl chlorides. Organic Letters. 5: 2505-7. PMID 12841766 DOI: 10.1021/Ol034775Z |
0.682 |
|
2003 |
Dastrup DM, VanBrunt MP, Weinreb SM. Preparation of bis(beta-trimethylsilylethanesulfonyl)imide and its use in the synthesis of protected amine derivatives. The Journal of Organic Chemistry. 68: 4112-5. PMID 12737604 DOI: 10.1021/Jo020754R |
0.501 |
|
2003 |
Artman GD, Weinreb SM. An approach to the total synthesis of the marine ascidian metabolite perophoramidine via a halogen-selective tandem Heck/carbonylation strategy. Organic Letters. 5: 1523-6. PMID 12713314 DOI: 10.1021/ol034314d |
0.804 |
|
2003 |
VanBrunt MP, Ambenge RO, Weinreb SM. A mild, convenient, and inexpensive procedure for conversion of vinyl halides to alpha-haloketones. The Journal of Organic Chemistry. 68: 3323-6. PMID 12688812 DOI: 10.1021/Jo020739M |
0.421 |
|
2003 |
Weinreb SM. Lepadiformine: a case study of the value of total synthesis in natural product structure elucidation. Accounts of Chemical Research. 36: 59-65. PMID 12534305 DOI: 10.1021/Ar0200403 |
0.362 |
|
2003 |
Weinreb SM, Chase CE, Wipf P, Venkatraman S. 2‐Trimethylsilylethanesulfonyl Chloride (SES‐Cl) Organic Syntheses. 161-161. DOI: 10.1002/0471264180.Os075.20 |
0.533 |
|
2002 |
Sun P, Sun C, Weinreb SM. 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. The Journal of Organic Chemistry. 67: 4337-45. PMID 12054972 DOI: 10.1021/Jo0201070 |
0.723 |
|
2002 |
Heintzelman GR, Fang WK, Keen SP, Wallace GA, Weinreb SM. Stereoselective total syntheses and reassignment of stereochemistry of the freshwater cyanobacterial hepatotoxins cylindrospermopsin and 7-epicylindrospermopsin. Journal of the American Chemical Society. 124: 3939-45. PMID 11942831 DOI: 10.1021/Ja020032H |
0.488 |
|
2002 |
Artman GD, Waldman JH, Weinreb SM. β-tosylethylhydroxylamine: Preparation and use as a hydroxylamine equivalent in amidyl radical-olefin cyclizations Synthesis. 2057-2063. DOI: 10.1055/S-2002-34371 |
0.771 |
|
2001 |
Sun P, Sun C, Weinreb SM. A new total synthesis of the marine tunicate alkaloid lepadiformine. Organic Letters. 3: 3507-10. PMID 11678694 DOI: 10.1021/Ol010179Y |
0.729 |
|
2001 |
Heintzelman GR, Fang WK, Keen SP, Wallace GA, Weinreb SM. Stereoselective total synthesis of the cyanobacterial hepatotoxin 7-epicylindrospermopsin: revision of the stereochemistry of cylindrospermopsin. Journal of the American Chemical Society. 123: 8851-3. PMID 11535093 DOI: 10.1021/ja011291u |
0.367 |
|
2001 |
Artman GD, Bartolozzi A, Franck RW, Weinreb SM. Preparation of N-sulfonylimines bearing easily removable protecting groups via the hudson reaction of oximes with sulfinyl chlorides Synlett. 232-233. DOI: 10.1055/S-2001-10783 |
0.77 |
|
2001 |
Lin X, Weinreb SM. Model studies on total synthesis of the chartellines, spirocyclic β-lactam alkaloids from a marine bryozoan Tetrahedron Letters. 42: 2631-2633. DOI: 10.1016/S0040-4039(01)00270-2 |
0.545 |
|
2001 |
Lin X, Artman GD, Stien D, Weinreb SM. Development of efficient new methodology for generation, cyclization and functional trapping of iminyl and amidyl radicals Tetrahedron. 57: 8779-8791. DOI: 10.1016/S0040-4020(01)00878-X |
0.803 |
|
2000 |
Bland DC, Raudenbush BC, Weinreb SM. Methodology for regioselective synthesis of substituted pyridines via intramolecular oximino malonate hetero Diels-Alder reactions. Organic Letters. 2: 4007-9. PMID 11112629 DOI: 10.1021/Ol006575I |
0.482 |
|
2000 |
Han G, LaPorte MG, Folmer JJ, Werner KM, Weinreb SM. Total syntheses of the Securinega alkaloids (+)-14,15-dihydronorsecurinine, (-)-norsecurinine, and phyllanthine. The Journal of Organic Chemistry. 65: 6293-306. PMID 11052071 DOI: 10.1021/Jo000260Z |
0.781 |
|
2000 |
Gastaldi S, Weinreb SM, Stien D. Diiodosilane: A reagent for mild, efficient conversion of carbamates to ureas via isocyanates The Journal of Organic Chemistry. 65: 3239-40. PMID 10814225 DOI: 10.1021/Jo9919714 |
0.368 |
|
2000 |
Han G, LaPorte MG, Folmer JJ, Werner KM, Weinreb SM. A New Enantioselective Approach to Total Synthesis of the Securinega Alkaloids: Application to (-)-Norsecurinine and Phyllanthine. Angewandte Chemie (International Ed. in English). 39: 237-240. PMID 10649387 DOI: 10.1002/(Sici)1521-3773(20000103)39:1<237::Aid-Anie237>3.0.Co;2-B |
0.761 |
|
2000 |
Chao W, Weinreb SM. Radical-based methodology for efficient generation of acyclic N-acylimines Tetrahedron Letters. 41: 9199-9204. DOI: 10.1016/S0040-4039(00)01683-X |
0.611 |
|
2000 |
Lin X, Stien D, Weinreb SM. A mild new procedure for production, cyclization and trapping of amidyl radicals: Application to a formal total synthesis of peduncularine Tetrahedron Letters. 41: 2333-2337. DOI: 10.1016/S0040-4039(00)00194-5 |
0.638 |
|
1999 |
Werner KM, de Los Santos JM, Weinreb SM, Shang M. An Intramolecular Nitrone-Olefin Dipolar Cycloaddition-Based Approach to Total Synthesis of the Cylindricine and Lepadiformine Marine Alkaloids. The Journal of Organic Chemistry. 64: 4865-4873. PMID 11674563 DOI: 10.1021/Jo990266S |
0.51 |
|
1999 |
Werner KM, de Los Santos JM, Weinreb SM, Shang M. A Convergent Stereoselective Synthesis of the Putative Structure of the Marine Alkaloid Lepadiformine via an Intramolecular Nitrone/1,3-Diene Dipolar Cycloaddition. The Journal of Organic Chemistry. 64: 686-687. PMID 11674128 DOI: 10.1021/Jo981897+ |
0.462 |
|
1999 |
Lin X, Stien D, Weinreb SM. A new method for the generation and cyclization of iminyl radicals via the Hudson reaction. Organic Letters. 1: 637-9. PMID 10823192 DOI: 10.1021/Ol990720E |
0.609 |
|
1999 |
Irie O, Samizu K, Henry JR, Weinreb SM. Further studies on total synthesis of sarain A. Efforts toward annulation of the macrocyclic rings Journal of Organic Chemistry. 64: 587-595. DOI: 10.1021/jo981821d |
0.371 |
|
1999 |
Stien D, Anderson GT, Chase CE, Koh YH, Weinreb SM. Total synthesis of the antitumor marine sponge alkaloid agelastatin A Journal of the American Chemical Society. 121: 9574-9579. DOI: 10.1021/Ja992487L |
0.545 |
|
1998 |
Kropf JE, Weinreb SM. Enantioselective intramolecular cyclizations of prochiral cyclohexanones using chiral lithium amide bases Chemical Communications. 2357-2358. DOI: 10.1039/A807052K |
0.815 |
|
1998 |
Anderson GT, Chase CE, Koh YH, Stien D, Weinreb SM, Shang M. Studies on total synthesis of the cytotoxic marine alkaloid agelastatin A Journal of Organic Chemistry. 63: 7594-7595. DOI: 10.1021/jo981785i |
0.33 |
|
1997 |
Sun P, Weinreb SM, Shang M. tert-Butylsulfonyl (Bus), a New Protecting Group for Amines. The Journal of Organic Chemistry. 62: 8604-8608. PMID 11672017 DOI: 10.1021/Jo971455I |
0.529 |
|
1997 |
Matzanke N, Gregg RJ, Weinreb SM, Parvez M. A Concise Approach to the Tricyclic Core of the Cytotoxic Marine Alkaloid Madangamine A. The Journal of Organic Chemistry. 62: 1920-1921. PMID 11671490 DOI: 10.1021/jo970208b |
0.676 |
|
1997 |
Jin J, Weinreb SM. Application of a stereospecific intramolecular allenylsilane imino ene reaction to enantioselective total synthesis of the 5,11- methanomorphanthridine class of Amaryllidaceae alkaloids Journal of the American Chemical Society. 119: 5773-5784. DOI: 10.1021/ja970839n |
0.344 |
|
1997 |
Jin J, Weinreb SM. Enantioselective total syntheses of the 5,11-methanomorphanthridine Amaryllidaceae alkaloids (-)-pancracine and (-)-coccinine Journal of the American Chemical Society. 119: 2050-2051. DOI: 10.1021/ja963900h |
0.362 |
|
1996 |
Heintzelman GR, Weinreb SM, Parvez M. Imino Diels-Alder-Based Construction of a Piperidine A-Ring Unit for Total Synthesis of the Marine Hepatotoxin Cylindrospermopsin. The Journal of Organic Chemistry. 61: 4594-4599. PMID 11667385 |
0.36 |
|
1996 |
Han G, LaPorte MG, McIntosh MC, Weinreb SM, Parvez M. Exploratory synthetic studies of the α-methoxylation of amides via cuprous ion-promoted decomposition of o-diazobenzamides Journal of Organic Chemistry. 61: 9483-9493. DOI: 10.1021/Jo961529A |
0.722 |
|
1996 |
Anderson GT, Alexander MD, Taylor SD, Smithrud DB, Benkovic SJ, Weinreb SM. Catalytic antibodies in synthesis: Design and synthesis of a hapten for application to the preparation of a scalemic pyrrolidine ring synthon for ptilomycalin A Journal of Organic Chemistry. 61: 125-132. DOI: 10.1021/Jo951469T |
0.308 |
|
1995 |
Borzilleri RM, Weinreb SM, Parvez M. Total synthesis of the unusual marine alkaloid (-)-papuamine utilizing a novel imino ene reaction Journal of the American Chemical Society. 117: 10905-10913. DOI: 10.1021/ja00149a013 |
0.379 |
|
1994 |
Borzilleri RM, Weinreb SM, Parvez M. Total synthesis of papuamine via a stereospecific intramolecular imino ene reaction of an allenylsilane Journal of the American Chemical Society. 116: 9789-9790. DOI: 10.1021/ja00100a070 |
0.369 |
|
1994 |
Han G, McIntosh MC, Weinreb SM. A convenient synthetic method for amide oxidation Tetrahedron Letters. 35: 5813-5816. DOI: 10.1016/S0040-4039(00)78191-3 |
0.377 |
|
1994 |
Larock RC, Yang H, Weinreb SM, Herr RJ. Synthesis of pyrrolidines and piperidines via palladium-catalyzed coupling of vinylic halides and olefinic sulfonamides Journal of Organic Chemistry. 59: 4172-4178. |
0.352 |
|
1993 |
Heintzelman GR, Parvez M, Weinreb SM. A Model Study on the Synthesis of the Marine Hepatotoxin Cylindrospermopsin Synlett. 1993: 551-552. DOI: 10.1055/S-1993-22524 |
0.359 |
|
1993 |
Henry JR, Weinreb SM. A convenient, mild method for oxidative cleavage of alkenes with Jones reagent/osmium tetraoxide Journal of Organic Chemistry. 58: 4745. DOI: 10.1021/Jo00069A047 |
0.372 |
|
1993 |
Folmer JJ, Weinreb SM. Generation of esters from carboxylic acids using Appel's salt (4,5-dichloro-1,2,3-dithiazolium chloride) Tetrahedron Letters. 34: 2737-2740. DOI: 10.1016/S0040-4039(00)73549-0 |
0.366 |
|
1993 |
Harris GD, Herr RJ, Weinreb SM. Synthesis of bicyclic nitrogen compounds via tandem intramolecular Heck cyclization and subsequent trapping of intermediate π-allylpalladium complexes Journal of Organic Chemistry. 58: 5452-5464. |
0.356 |
|
1991 |
McIntosh MC, Weinreb SM. A strategy for synthesis of conduritols and related cyclitols via stereodivergent vinylsilane-aldehyde cyclizations Journal of Organic Chemistry. 56: 5010-5012. DOI: 10.1021/Jo00017A005 |
0.448 |
|
1991 |
Bell SI, Parvez M, Weinreb SM. Metalation and alkylation of 3,6-dihydrothiazine 1-oxides prepared via Diels-Alder cycloadditions of N-sulfinyl dienophiles Journal of Organic Chemistry. 56: 373-377. DOI: 10.1021/Jo00001A068 |
0.358 |
|
1989 |
Subramanyam C, Noguchi M, Weinreb SM. An approach to amphimedine and related marine alkaloids utilizing an intramolecular Kondrat'eva pyridine synthesis Journal of Organic Chemistry. 54: 5580-5585. |
0.313 |
|
1988 |
Melnick MJ, Freyer AJ, Weinreb SM. Generation and intramolecular cationic cyclizations of N-tosylimines derived from enolizable aldehydes Tetrahedron Letters. 29: 3891-3894. DOI: 10.1016/S0040-4039(00)80373-1 |
0.307 |
|
1988 |
Turos E, Parvez M, Garigipati RS, Weinreb SM. An attempted synthesis of biotin Journal of Organic Chemistry. 53: 1116-1118. |
0.318 |
|
1987 |
Joyce RP, Gainor JA, Weinreb SM. Synthesis of the aromatic and monosaccharide moieties of staurosporine Journal of Organic Chemistry. 52: 1177-1185. |
0.4 |
|
1987 |
Natsugari H, Turos E, Weinreb SM, Cvetovich RJ. Further studies on stereoselective synthesis of vicinal diamines from 3,6-dihydrothiazine-1-imines Heterocycles. 25: 19-24. |
0.396 |
|
1986 |
Garigipati RS, Cordova R, Parvez M, Weinreb SM. Diastereoselective synthesis of highly functionalized homoallylic amine derivatives via diels-alder adducts of N-sulfinyl dienophiles Tetrahedron. 42: 2979-2983. DOI: 10.1016/S0040-4020(01)90588-5 |
0.35 |
|
1986 |
Scola PM, Weinreb SM. Synthetic and stereochemical aspects of intramolecular [4 + 2] cycloadditions of N-acyl iminium compounds with alkene and alkyne dienophiles Journal of Organic Chemistry. 51: 3248-3250. |
0.32 |
|
1985 |
Weinreb SM. Alkaloid total synthesis by intramolecular imino Diels-Alder cycloadditions Accounts of Chemical Research. 18: 16-21. |
0.421 |
|
1985 |
Garigipati RS, Tschaen DM, Weinreb SM. Total synthesis of (+)-actinobolin Journal of the American Chemical Society. 107: 7790-7792. |
0.318 |
|
1984 |
Dodd JH, Starrett JE, Weinreb SM. Total synthesis of tri-O-methylolivin Journal of the American Chemical Society. 106: 1811-1812. DOI: 10.1021/Ja00318A043 |
0.329 |
|
1984 |
Levin JI, Weinreb SM. Synthesis of eupolauramine via an intramolecular Kondrat'eva pyridine synthesis Journal of Organic Chemistry. 49: 4325-4332. |
0.371 |
|
1984 |
Bailey TR, Garigipati RS, Morton JA, Weinreb SM. Total synthesis of anhydrocannabisativene Journal of the American Chemical Society. 106: 3240-3245. |
0.318 |
|
1984 |
Natsugari H, Whittle RR, Weinreb SM. Stereocontrolled synthesis of unsaturated vicinal diamines from Diels-Alder adducts of sulfur dioxide bis(imides) Journal of the American Chemical Society. 106: 7867-7872. |
0.43 |
|
1984 |
Remiszewski SW, Whittle RR, Weinreb SM. Synthesis of 5-epi-desosamine via a stereoselective intramolecular N-sulfinyl Diels-Alder cycloaddition Journal of Organic Chemistry. 49: 3243-3244. |
0.367 |
|
1983 |
Bremmer ML, Khatri NA, Weinreb SM. Quinolizidine alkaloid synthesis via the intramolecular imino Diels-Alder reaction. epi-lupinine and cryptopleurine Journal of Organic Chemistry. 48: 3661-3666. DOI: 10.1021/Jo00169A009 |
0.477 |
|
1983 |
Levin JI, Weinreb SM. Total synthesis of eupolauramine Journal of the American Chemical Society. 105: 1397-1398. DOI: 10.1021/Ja00343A068 |
0.43 |
|
1983 |
Bremmer ML, Weinreb SM. A stereoselective total synthesis of epi-lupinine Tetrahedron Letters. 24: 261-264. DOI: 10.1016/S0040-4039(00)81380-5 |
0.363 |
|
1982 |
Weinreb SM, Levin JI, Turos E. An Alternative Procedure for the Aluminum-Mediated Conversion of Esters to Amides Synthetic Communications. 12: 989-993. DOI: 10.1080/00397918208061938 |
0.66 |
|
1982 |
Dodd JH, Garigipati RS, Weinreb SM. Development of a strategy for convergent total synthesis of the aureolic acid antitumor antibiotics Journal of Organic Chemistry. 47: 4045-4049. DOI: 10.1021/Jo00142A009 |
0.345 |
|
1982 |
Weinreb SM, Basha FZ, Hibino S, Khatri NA, Kim D, Pye WE, Wu TT. Total synthesis of the antitumor antibiotic streptonigrin Journal of the American Chemical Society. 104: 536-544. DOI: 10.1021/Ja00366A028 |
0.67 |
|
1982 |
Levin JI, Weinreb SM. A novel ring cleavage reaction of oxazolines Tetrahedron Letters. 23: 2347-2350. DOI: 10.1016/S0040-4039(00)87338-4 |
0.327 |
|
1982 |
Garigipati RS, Morton JA, Weinreb SM. A method for diastereoselective synthesis of unsaturated acyclic amines Tetrahedron Letters. 24: 987-990. DOI: 10.1016/S0040-4039(00)81583-X |
0.338 |
|
1982 |
Weinreb SM, Staib RR. Synthetic aspects of diels-alder cycloadditions with heterodienophiles Tetrahedron. 38: 3087-3128. DOI: 10.1016/0040-4020(82)80047-1 |
0.355 |
|
1981 |
Khatri NA, Schmitthenner HF, Shringarpure J, Weinreb SM. Synthesis of indolizidine alkaloids via the intramolecular imino Diels-Alder reaction Journal of the American Chemical Society. 103: 6387-6393. |
0.372 |
|
1980 |
Basha FZ, Hibino S, Kim D, Pye WE, Wu TT, Weinreb SM. Total synthesis of streptonigrin [12] Journal of the American Chemical Society. 102: 3962-3964. |
0.317 |
|
1980 |
Schmitthenner HF, Weinreb SM. Total synthesis of elaeokanine A Journal of Organic Chemistry. 45: 3372-3373. |
0.318 |
|
1979 |
Weinreb SM, Khatri NA, Shringarpure J. Alkaloid synthesis by the intramolecular imino Diels-Alder reaction. .delta.-Coniceine and tylophorine Journal of the American Chemical Society. 101: 5073-5074. DOI: 10.1021/Ja00511A052 |
0.476 |
|
1979 |
Kim MY, Weinreb SM. Construction of an isoindolone precursor for synthesis of the macrolactone cytochalasins Tetrahedron Letters. 20: 579-582. DOI: 10.1016/S0040-4039(01)86006-8 |
0.324 |
|
1979 |
Weinreb SM, Khatri NA, Shringarpure J. Alkaloid synthesis by the intramolecular imino Diels-Alder reaction. .delta.-Coniceine and tylophorine Cheminform. 10. DOI: 10.1002/Chin.197948353 |
0.476 |
|
1979 |
Weinreb SM, Khatri NA, Shringarpure J. Alkaloid synthesis by the intramolecular imino Diels-Alder reaction. δ-Coniceine and tylophorine [11] Journal of the American Chemical Society. 101: 5073-5074. |
0.379 |
|
1978 |
Hatch RP, Shringarpure J, Weinreb SM. Studies on total synthesis of the olivomycins Journal of Organic Chemistry. 43: 4172-4177. |
0.316 |
|
1976 |
Cole RJ, Kirksey JW, Clardy J, Eickman N, Weinreb SM, Singh P, Kim D. Structures of rugulovasine-A and -B and 8-chlororugulovasine-A and -B Tetrahedron Letters. 17: 3849-3852. DOI: 10.1016/0040-4039(76)80164-5 |
0.584 |
|
1975 |
Weinreb SM, Auerbach J. Total synthesis of the cephalotaxus alkaloids. Cephalotaxine, cephalotaxinone, and demethylcephalotaxinone. Journal of the American Chemical Society. 97: 2507-16. PMID 1133419 DOI: 10.1002/Chin.197529425 |
0.447 |
|
1975 |
Weinreb SM, Semmelhack MF. Synthesis of the Cephalotaxus alkaloids Accounts of Chemical Research. 8: 158-164. DOI: 10.1002/Chin.197535390 |
0.351 |
|
1972 |
Auerbach J, Weinreb SM. The total synthesis of cephalotaxine. Journal of the American Chemical Society. 94: 7172-3. PMID 5072334 |
0.318 |
|
1971 |
Büchi G, Klaubert DH, Shank RC, Weinreb SM, Wogan GN. Structure and synthesis of kotanin and desmethylkotanin, metabolites of Aspergillus glaucus. The Journal of Organic Chemistry. 36: 1143-7. PMID 5551701 |
0.563 |
|
1971 |
Büchi G, Weinreb SM. Total syntheses of aflatoxins M1 and G1 and an improved synthesis of aflatoxin B1. Journal of the American Chemical Society. 93: 746-52. PMID 5545312 |
0.528 |
|
1969 |
Büchi G, Weinreb SM. The total synthesis of racemic aflatoxin-M1 (milk toxin). Journal of the American Chemical Society. 91: 5408-9. PMID 5816760 |
0.54 |
|
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