1994
DOI: 10.1016/0032-3861(94)90321-2
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Solid-phase synthesis of oligoethers: soluble polymer model studies

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Cited by 7 publications
(4 citation statements)
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“…Template attachment to pre-formed polymer resins: In the next step the functionalised protected quinine 1.6 and quinidine 2.4 were attached via an ether linkage to the in-house prepared VBC-containing resins (Scheme 3). [50,51,53,75] The use of microwave reactor vessels proved advantageous for small scale reactions, while for larger scale reactions A C H T U N G T R E N N U N G (>500 mg) a classical experimental set up [76][77][78] using a threenecked, round-bottomed flask with nitrogen inlet, condenser and mechanical stirrer was a better choice. Cleavage of the tert-butyldimethylsilyl ether was carried out at room temperature in sealed glass vials on flatbed rollers for 24 h.…”
Section: Resinmentioning
confidence: 99%
“…Template attachment to pre-formed polymer resins: In the next step the functionalised protected quinine 1.6 and quinidine 2.4 were attached via an ether linkage to the in-house prepared VBC-containing resins (Scheme 3). [50,51,53,75] The use of microwave reactor vessels proved advantageous for small scale reactions, while for larger scale reactions A C H T U N G T R E N N U N G (>500 mg) a classical experimental set up [76][77][78] using a threenecked, round-bottomed flask with nitrogen inlet, condenser and mechanical stirrer was a better choice. Cleavage of the tert-butyldimethylsilyl ether was carried out at room temperature in sealed glass vials on flatbed rollers for 24 h.…”
Section: Resinmentioning
confidence: 99%
“…Nevertheless there are situations where linear soluble polymers can be extremely useful and a key factor in this is that chemical reactions performed on such polymers can be a d for polystyrene and styrene-divinylbenzene copolymers is ~17-18 (MPa) 0.5 monitored by, for example, high resolution solution phase 1 H and 13 C NMR spectroscopy. 15 Though the resonances due to backbone protons are usually broadened, signals arising from mobile groups in the sidechain are often as sharp as resonances from analogous low molecular weight groups in isotropic solution. Recently, however, considerable advances have also been made in 1 H and 13 C NMR analysis of crosslinked polymers 16 (see later).…”
Section: Soluble Polymer Supportsmentioning
confidence: 99%
“…As well as particular peptides, generally with some potential biological activity associated with them, interest has grown in synthesising glycopeptides. The problems of extending the concept to oligoether synthesis, which at first sight seems simple, have also been highlighted [82].…”
Section: Polymeric Protecting Groupsmentioning
confidence: 99%