Total synthesis of pseudolaric acid A.
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[1] B. Trost,et al. Total synthesis of (-)-pseudolaric acid B. , 2007, Journal of the American Chemical Society.
[2] Jian Ding,et al. Pseudolarix Acid B, a New Tubulin-Binding Agent, Inhibits Angiogenesis by Interacting with a Novel Binding Site on Tubulin , 2006, Molecular Pharmacology.
[3] A. Padwa. The interaction of rhodium carbenoids with carbonyl compounds as a method for the synthesis of tetrahydrofurans , 2005 .
[4] J. Lex,et al. Total synthesis of (-)-colchicine via a Rh-triggered cycloaddition cascade. , 2005, Organic letters.
[5] A. Gupta,et al. Rhodium-catalyzed tandem cyclization-cycloaddition reactions of enynebenzaldehydes: construction of polycyclic ring systems. , 2005, Chemical communications.
[6] L. Chow,et al. Pseudolaric Acid B, a Novel Microtubule-Destabilizing Agent That Circumvents Multidrug Resistance Phenotype and Exhibits Antitumor Activity In vivo , 2005, Clinical Cancer Research.
[7] P. Rashatasakhon,et al. Efficient construction of the oxatricyclo[6.3.1.0(0,0)]dodecane core of komaroviquinone using a cyclization/cycloaddition cascade of a rhodium carbenoid intermediate. , 2005, Organic letters.
[8] P. Chiu. Application of the carbene cyclization-cycloaddition cascade in total synthesis , 2005 .
[9] T. Ikejima,et al. Pseudolaric acid B induces apoptosis via activation of c-Jun N-terminal kinase and caspase-3 in HeLa cells , 2004, Experimental & Molecular Medicine.
[10] Z. Miao,et al. Pseudolaric Acid B Inhibits Angiogenesis and Reduces Hypoxia-Inducible Factor 1α by Promoting Proteasome-Mediated Degradation , 2004, Clinical Cancer Research.
[11] Yi Chen,et al. Pseudolarix acid B inhibits angiogenesis by antagonizing the vascular endothelial growth factor-mediated anti-apoptotic effect. , 2004, European journal of pharmacology.
[12] E. Suresh,et al. Regioselective synthesis of mono- and bis-decahydrobenzocarbazoles via tandem reactions of α-diazo ketones , 2004 .
[13] D. M. Hodgson,et al. Use of allene in 1,3-dipolar addition to a carbonyl ylide: syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid. , 2004, Chemical communications.
[14] S. Kitagaki,et al. Total synthesis of the squalene synthase inhibitor zaragozic acid C by a carbonyl ylide cycloaddition strategy. , 2003, Angewandte Chemie.
[15] P. Chiu,et al. A tandem metal carbene cyclization-cycloaddition approach to the pseudolaric acids. , 2003, The Journal of organic chemistry.
[16] G. Mehta,et al. Tandem cyclization–cycloaddition reactions of rhodium generated carbenoids from α-diazo carbonyl compounds , 2002 .
[17] D. Noonan,et al. Pseudolaric acid analogs as a new class of peroxisome proliferator-activated receptor agonists. , 2002, Planta medica.
[18] H. Tokuyama,et al. Reduction of ethanethiol esters to aldehydes , 2002 .
[19] J. Karle,et al. Toward the total synthesis of pseudolaric acid B. Preparation of a key intermediate by degradation and its use in the reassembly of the natural product , 2002 .
[20] P. Chiu,et al. A rhodium carbene cyclization-cycloaddition cascade strategy toward the pseudolaric acids. , 2001, Organic letters.
[21] Guoqiang Song,et al. Diastereoselective intramolecular [4+3] cycloaddition: Synthesis of a versatile precursor for preparation of 5,7-fused ring compounds , 1999 .
[22] S. Kitagaki,et al. Enantiocontrol in Tandem Carbonyl Ylide Formation and Intermolecular 1,3-Dipolar Cycloaddition of α-Diazo Ketones Mediated by Chiral Dirhodium(II) Carboxylate Catalyst , 1999 .
[23] Davidr . Evans,et al. C2-Symmetric Copper(II) Complexes as Chiral Lewis Acids. Scope and Mechanism of Catalytic Enantioselective Aldol Additions of Enolsilanes to (Benzyloxy)acetaldehyde , 1999 .
[24] Davidr . Evans,et al. C2-Symmetric Copper(II) Complexes as Chiral Lewis Acids. Scope and Mechanism of the Catalytic Enantioselective Aldol Additions of Enolsilanes to Pyruvate Esters , 1999 .
[25] Youhong Hu,et al. The synthesis of a 5,7-membered fused-ring compound by a tandem Pummerer rearrangement and intramolecular [4+3] cycloaddition , 1999 .
[26] P. Chiu,et al. A conjugate reduction-intramolecular aldol strategy toward the synthesis of pseudolaric acid A , 1998 .
[27] A. Padwa. The domino cycloaddition/N-acyliminium ion cyclization cascade , 1998 .
[28] T. Ye,et al. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds: From Cyclopropanes to Ylides , 1998 .
[29] A. Tebbe,et al. The First Synthesis of a Daphnane Diterpene: The Enantiocontrolled Total Synthesis of (+)-Resiniferatoxin , 1997 .
[30] A. Padwa. Tandem Processes of Metallo Carbenoids for the Synthesis of Azapolycycles , 1997 .
[31] B. M. T. and,et al. On the Diastereoselectivity of Intramolecular Pd-Catalyzed TMM Cycloadditions. An Asymmetric Synthesis of the Perhydroazulene (−)-Isoclavukerin A , 1996 .
[32] J. Winkler. Tandem Diels−Alder Cycloadditions in Organic Synthesis , 1996 .
[33] A. Padwa,et al. Cascade Processes of Metallo Carbenoids. , 1996, Chemical reviews.
[34] P. Parsons,et al. Tandem Reactions in Organic Synthesis: Novel Strategies for Natural Product Elaboration and the Development of New Synthetic Methodology. , 1996, Chemical reviews.
[35] A. Clark,et al. Antifungal evaluation of pseudolaric acid B, a major constituent of Pseudolarix kaempferi. , 1995, Journal of natural products.
[36] J. Olive,et al. .alpha.-Hydroxy esters as chiral auxiliaries in asymmetric cyclopropanations by rhodium(II)-stabilized vinylcarbenoids , 1993 .
[37] L. Tietze,et al. Sequential Transformations in Organic Chemistry: A Synthetic Strategy with a Future† , 1993 .
[38] L. Tietze,et al. Sequentielle Transformationen in der Organischen Chemie eine Synthesestrategie mit Zukunft , 1993 .
[39] S. Condon,et al. Allylsilane-based annulations. Direct stereoselective syntheses of (.+-.)-graveolide and (.+-.)-aromaticin , 1992 .
[40] T. Ye,et al. Synthesis of chiral n-protected α-amino-β-diketones from α-diazoketones derived from natural amino acids , 1992 .
[41] C. Schmid,et al. 2,3-O-(3-Pentylidene)-D-glyceraldehyde and 2,3-O-(3-Pentylidene)-L-glyceraldehyde: Convenient Glyceraldehyde Surrogates Obtained via a Novel Periodate-Based Oxdation System , 1992 .
[42] M. Harmata,et al. Alkoxyvinyl thionium ions in intramolecular 4 + 3 cycloaddition reactions , 1991 .
[43] Z. Gu,et al. [Effects of pseudolaric acid B on blood flows of endometrium and myometrium in pregnant rats]. , 1991, Zhongguo yao li xue bao = Acta pharmacologica Sinica.
[44] A. Padwa,et al. Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairs , 1991 .
[45] T. Fukuyama,et al. Facile reduction of ethyl thiol esters to aldehydes: application to a total synthesis of (+)-neothramycin A methyl ether , 1990 .
[46] G. Cordell,et al. Pseudolaric acid B: NMR assignments, conformational analysis and cytotoxicity , 1989 .
[47] Cai Guo-lin,et al. Synthetic studies on pseudolaric acid A , 1989 .
[48] Z. Yoshida,et al. Unsaturated ester synthesis via copper(I)-catalyzed allylation of zinc esters , 1987 .
[49] S. Bromidge,et al. Total synthesis of (±)-β-bulnesene via intramolecular cycloaddition of a 2-substituted 3-oxidopyrylium , 1985 .
[50] Y. Yan,et al. Pseudolaric Acids from Pseudolarix kaempferi , 1983, Planta medica.
[51] Y. Z. Zhu,et al. [Antifertility effect of pseudolaric acid B]. , 1982, Zhongguo yao li xue bao = Acta pharmacologica Sinica.
[52] G. Cahiez,et al. Derives organomagnesiens ω-alcoolates: Preparation et proprietes , 1978 .
[53] J. Normant,et al. Substitution directe de l'halogène d'halohydrines 1-2 par des organomagnésiens et lithiens en présence de sel cuivreux , 1978 .