New Synthetic Method for Functionalized Pyrrolizidine, Indolizidine, and Mitomycin Alkaloids
- 1 August 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (34) , 8127-8128
- https://doi.org/10.1021/ja9716564
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Facile Preparation of Cyclopropylamines from CarboxamidesThe Journal of Organic Chemistry, 1997
- Selective cleavage of allyl ethersTetrahedron Letters, 1996
- A New Variant of the Kulinkovich Hydroxycyclopropanation. Reductive Coupling of Carboxylic Esters with Terminal OlefinsJournal of the American Chemical Society, 1996
- A New Preparation of Cyclopropanone Hemiketals by Reductive Coupling of Terminal Olefins with Ethylene CarbonateThe Journal of Organic Chemistry, 1996
- Intramolecular Hydroxycyclopropanation of ω-Vinyl Carboxylic EstersJournal of the American Chemical Society, 1996
- Practical total synthesis of (.+-.)-mitomycin CJournal of the American Chemical Society, 1989
- Total synthesis of (.+-.)-mitomycins via isomitomycin AJournal of the American Chemical Society, 1987
- The Total Synthesis of MitomycinsJournal of Natural Products, 1979
- Synthetiic studies toward mitomycins. III. Total syntheses of mitomycins A and CTetrahedron Letters, 1977
- Synthetic studies toward mitomycins. 2. Total synthesis of dl-porfiromycinJournal of the American Chemical Society, 1977