A New Variant of the Baylis-Hillman Reaction for Solid Phase Organic Synthesis.

Ulrich Reiser; Johann Jauch

doi:10.3390/ecsoc-4-01888

x Selected file doesn't exist!

Previous Article in event

Scope and Limitation of a Tin Promoted Amidation on Solid Phase: A New Monitoring for the T1 Triazene Linker

Next Article in event

Hydroxy-(2-chlorophenyl)methyl Polystyrene Resin: Studies on the Immobilization and Cleavage of Acids and Alcohols

A New Variant of the Baylis-Hillman Reaction for Solid Phase Organic Synthesis.

Ulrich Reiser

Johann Jauch

¹ Institut für Organische Chemie und Biochemie, Technische Universität München, Lichtenbergstr. 4, D-85747 Garching, Germany.

Published: 11 September 2000 by MDPI in The 4th International Electronic Conference on Synthetic Organic Chemistry session Solid Phase Chemistry and Combinatorial Synthesis

https://doi.org/10.3390/ecsoc-4-01888

Abstract: A new variant of the Baylis-Hillman reaction based on lithium phenylselenide is adapted to Solid Phase Organic Synthesis (SPOS). Scope and limitations are studied using four polymer bound aldehydes.

Keywords: Solid phase synthesis, Baylis-Hillman reactions.

View paper

59 Reads
0 Recommendations

Ulrich Reiser

Johann Jauch