636596-82-2Relevant articles and documents
Highly stereoselective and stereodivergent synthesis of four types of THF cores in acetogenins using a C4-chiral building block
Maezaki, Naoyoshi,Kojima, Naoto,Asai, Mikito,Tominaga, Hiroaki,Tanaka, Tetsuaki
, p. 2977 - 2980 (2002)
(Formula Presented) Four stereoisomers of the THF cores, synthetic intermediates of acetogenins, have been synthesized with high diastereoselectivity by asymmetric alkynylation and subsequent stereodivergent THF ring formation. The asymmetric alkynylation
Systematic Construction of a Monotetrahydrofuran-Ring Library in Annonaceous Acetogenins by Asymmetric Alkynylation and Stereodivergent Tetrahydrofuran-Ring Formation
Kojima, Naoto,Maezaki, Naoyoshi,Tominaga, Hiroaki,Asai, Mikito,Yanai, Minori,Tanaka, Tetsuaki
, p. 4980 - 4990 (2007/10/03)
All eight diastereoisomers of the monotetrahydrofuran-ring cores of annonaceous acetogenins have been synthesized through utilization of asymmetric alkynylation and stereodivergent one-pot tetrahydrofuran-ring formation. In all cases, the asymmetric alkyn