158010-58-3Relevant academic research and scientific papers
Development of a Synthesis of Lankacidins: Stereoselective Synthesis of the δ-Lactone Fragment
Thomas, Eric J.,Williams, Andrew C.
, p. 351 - 358 (2007/10/02)
Electrophiles react at C(3) stereoselectively on the less hindered face of the enolate derived from the 4-substituted azetidinone 5 to give products in which the new substituent is trans to the (tert-butyldimethylsilyloxymethyl)group at C(4).Aldol additio
