Enantioselective synthesis of C3-C10 fragment (northeastern zone) of maytansinoids with 4-chiral centers (4S,5S,6R,7S)
- 1 January 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (40) , 3925-3928
- https://doi.org/10.1016/s0040-4039(01)82028-1
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- A highly efficient asymmetric synthesis of optically active α,β-epoxyaldehydes from α,β-unsaturated acidsTetrahedron Letters, 1980
- Total synthesis of (.+-.)-maytansinol. The common precursor to the maytansinoidsJournal of the American Chemical Society, 1980
- An equilibrium between carbene and a metal-carbene complex. Homogeneous catalysis by mercury(II)Journal of the American Chemical Society, 1980
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- The use of dithioesters as acyl anion equivalents. Double homologation of the synthon.Tetrahedron Letters, 1978
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978
- Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. An approach utilizing side chain synthons of microbiological originThe Journal of Organic Chemistry, 1976
- Preparation of L(+) β‐hydroxyisobutyric acid by bacterial oxidation of isobutyric acidBiotechnology & Bioengineering, 1971
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969