Macrocycles, 1. Macrocyclic polymerizations of (thio)lactones – stepwise ring expansion and ring contraction
✍ Scribed by Hans R. Kricheldorf; Soo-Ran Lee; Nicole Schittenhelm
- Book ID
- 102662035
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 735 KB
- Volume
- 199
- Category
- Article
- ISSN
- 1022-1352
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📜 SIMILAR VOLUMES
## A&Wrack Lactones and lactams 4-6 were synthesized from a series of acyclic dienes 1-3 via ringclosing olefin metathesis, as shown in equation 1. The geometry of the resulting double bond was determined, and the UZratios compared to values from molecular mechanics calculations.
At moderate temperatures the dimeric 2,2-dibutyl-2-stanna-1,3-dioxolane (DSDOL) and the monomeric 2,2-dibutyl-2-stanna-1,3-dioxepane (DSDOP) add to equivalents of succinic anhydride by a clean insertion reaction into the Sn1O bonds. The resulting 30-and 17-membered macrocycles are stable up to tempe
2-(3-Hydroxypropyl)-2-nitrocycloalkanones undergo base-catalysed isomerisation into nitro-lactones containing 'Theketo-lactones 5 have been made before by oxidation of the dihydropyrans 7 to the diols with moist peractic acid followed by treatment with lead tetra-acetate or by direct oxidation with