Title of article :
Methyl 3-bromomethyl-3-butenoate as an isopentane building block for the stereoselective preparation of (S)-4-methyl-3,6-dihydro-2H-pyran-2-carbaldehyde and (+)-faranal
Author/Authors :
Mineyeva، نويسنده , , Iryna V. and Kulinkovich، نويسنده , , Oleg G.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2010
Abstract :
(S)-4-Methyl-3,6-dihydro-2H-pyran-2-carbaldehyde (3), the common intermediate in the syntheses of the C17–C27 subunit of laulimalide (4) and (+)-faranal (5), the trail pheromone of the pharaoh ant, Monomorium pharaonis, were obtained via transformation of methyl 3-bromomethyl-3-butenoate (1) into allylstannane 2 and subsequent allylation of (benzyloxy)acetaldehyde (6) in accordance with the Keck procedure as the key steps.
Keywords :
cyclopropanols , asymmetric synthesis , Ring opening , (+)-Faranal , allyl halides
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters