21149-17-7Relevant articles and documents
Wojciechowska et al.
, p. 4063 (1978)
3-Imidoallenylphosphonates: In Situ Formation and β-Alkoxylation
Berton, Jan K. E. T.,Heugebaert, Thomas S. A.,Debrouwer, Wouter,Stevens, Christian V.
, p. 208 - 211 (2016)
3-Imidoallenylphosphonates, allenes bearing both an electron-withdrawing and -donating group, were isolated for the first time. An alkoxy substituent was introduced into these unprecedented intermediates in a one-pot approach, yielding β-functionalized am
Conjugate addition of ammo acid side chains to alkynones and alkynoic acid derivatives
Crisp, Geoffrey T.,Millan, Michael J.
, p. 637 - 648 (1998)
Suitably protected amino acids were used to investigate the Michael addition of the sulfanyl group of cysteine, the hydroxyl group of serine and the ε-amino group of lysine to a conjugated alkynone, alkynoic ester and alkynoic amide. The expected heterosu
SULFUR EXTRUSION FROM DISULFIDES BY CARBENES
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Page/Page column 30; 39-42, (2021/10/30)
The present invention relates to a method for preparing a compound T having a thioether group from a compound D having a disulfide group in the presence of a carbene.