74076-63-4Relevant articles and documents
Lewis Acid-Catalyzed Vinyl Acetal Rearrangement of 4,5-Dihydro-1,3-dioxepines: Stereoselective Synthesis of cis- And trans-2,3-Disubstituted Tetrahydrofurans
Ghosh, Arun K.,Belcher, Miranda R.
, p. 10399 - 10412 (2020/09/02)
Lewis acid-catalyzed rearrangements of 4,5-dihydro-1,3-dioxepines have been investigated. Rearrangement of vinyl acetals under a variety of conditions resulted in cis- and trans-2,3-disubstituted tetrahydrofuran derivatives in a highly stereoselective man
Synthesis of the first photo-triggered pro-mitosene based on FR-900482
Williams, Robert M.,Rollins, Samuel B.,Judd, Ted C.
, p. 521 - 532 (2007/10/03)
A stereocontrolled synthesis of an eight-membered ring precursor to a photo-triggered mitosene is described. (C) 2000 Elsevier Science Ltd.
STEREOSPECIFIC SYNTHESIS OF A RIBOSYL-DIAZEPANONE DERIVATIVE; A SYNTHETIC APPROACH FOR ELUCIDATION OF THE STEREOCHEMISTRY OF A LIPID NUCLEOSIDE ANTIBIOTIC LIPOSIDOMYCIN B
Spada, Marianne R.,Ubukata, Makoto,Isono, Kiyoshi
, p. 1147 - 1167 (2007/10/02)
A new type of ribosyl-diazepanone derivative (23), the core ribosyl 7-membered heterocycle of the nucleoside antibiotic liposidomycin B has been synthesized using a chiral synthetic route that could offer accessibility to any of possible stereoisomers of