A concise enantioselective total synthesis of rhizoxin D

[1]  K. Nacro,et al.  Attempt to rationalize the diastereoselectivity in the addition of ester enolate to optically active α,β-epoxyaldehydes , 1999 .

[2]  Michael G. Yang,et al.  Chelate-controlled carbonyl addition reactions. The exceptional chelating abilityof dimethylaluminum chloride and methylaluminum dichloride , 1999 .

[3]  S. Aamdal,et al.  Multicentre phase II pharmacological evaluation of rhizoxin. Eortc early clinical studies (ECSG)/pharmacology and molecular mechanisms (PAMM) groups. , 1996, British Journal of Cancer.

[4]  David R. Williams,et al.  Total synthesis of Rhizoxin D , 1996 .

[5]  Christopher D. J. Boden,et al.  Palladium-catalysed hydrostannylations of 1-bromoalkynes. A practical synthesis of (E)-1-stannylalk-1-enes , 1996 .

[6]  Michael G. Yang,et al.  Diastereoselective Aldol and Allylstannane Addition Reactions. The Merged Stereochemical Impact of .alpha. and .beta. Aldehyde Substituents , 1995 .

[7]  S. Iwasaki,et al.  The first total synthesis of the antitumor macrolide, rhizoxin , 1993 .

[8]  V. Farina,et al.  Large rate accelerations in the stille reaction with tri-2-furylphosphine and triphenylarsine as palladium ligands: mechanistic and synthetic implications , 1991 .

[9]  H. X. Zhang,et al.  Palladium- and molybdenum-catalyzed hydrostannation of alkynes: a novel access to regio- and stereodefined vinylstannanes , 1990 .

[10]  E. Carreira,et al.  Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride , 1988 .

[11]  K. Tomooka,et al.  Stereocontrolled asymmetric total synthesis of protomycinolide IV , 1986 .

[12]  M. Okuhara,et al.  A new antitumor complex, WF-1360, WF-1360A, B, C, D, E and F. , 1986, The Journal of antibiotics.

[13]  S. Iwasaki,et al.  Studies on macrocyclic lactone antibiotics. IX: Novel macrolides from the fungus Rhizopus chinensis: precursors of rhizoxin , 1986 .

[14]  A. Itai,et al.  Studies on macrocyclic lactone antibiotics. VIII. Absolute structures of rhizoxin and a related compound. , 1986, Journal of antibiotics (Tokyo. 1968).

[15]  Davidr . Evans,et al.  The directed reduction of β-hydroxy ketones employing Me4NHB(OAc)3 , 1986 .

[16]  Jeffery T. Davis,et al.  Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds , 1984 .

[17]  S. Iwasaki,et al.  Studies on macrocyclic lactone antibiotics. VII. Structure of a phytotoxin "rhizoxin" produced by Rhizopus chinensis. , 1984, The Journal of antibiotics.

[18]  T. Saegusa,et al.  Synthesis of .alpha.,.beta.-unsaturated carbonyl compounds by palladium(II)-catalyzed dehydrosilylation of silyl enol ethers , 1978 .

[19]  E. Corey,et al.  A key intermediate for the synthesis of maytansine and related antitumor agents , 1978 .