29336-32-1Relevant articles and documents
Synergistic Dual Directing Groups-Enabled Diastereoselective C-H Cyclopropylation via Rh(III)-Catalyzed Couplings with Cyclopropenyl Alcohols
Wu, Min,Lin, Shuang,Zhu, Guoxun,Sun, Ming,Zhou, Zhi,Gao, Hui,Yi, Wei
supporting information, (2020/02/25)
By using a synergistic dual directing group-assisted C-H activation strategy and simply modifying the reaction conditions, we realized a robust and general Cp*Rh(III)-catalyzed C-H cyclopropylation of N-acetoxybenzamides with cyclopropenyl alcohols, provi
Hypervalent iodine(III)-mediated oxidation of aldoximes to N-acetoxy or N-hydroxy amides
Ghosh, Harisadhan,Patel, Bhisma K.
experimental part, p. 384 - 390 (2010/02/15)
Treatment of various aliphatic and aromatic aldoximes with the hypervalent iodine(iii) reagents (diacetoxyiodo)benzene (DIB) or Koser's reagent [hydroxy(tosyloxy)iodo]benzene (HTIB) gave, respectively, N-acetoxy or N-hydroxy amides in good yields rather t
Regio-selective formation of O-acyl/O-benzoyl hydroxamates by using a polymer supported reagent strategy
Burungule,Bondge,Munde,Bhingolikar,Mane
, p. 1923 - 1927 (2007/10/03)
Rapid, quantitative and regioselective O-acylation/O-benzoylation of hydroxamic acids has been carried using polymer supported hydroxamate anions and acetyl/benzoyl chloride under mild conditions. The isolation of unambiguous and pure products by si-mple
