Betylates. 3. Preparative nucleophilic substitution by way of [2]-, [3]-, and [4]betylates. Stoichiometric phase transfer and substrate-reagent ion-pair (SRIP) reactions of betylates
Betylates. 3. Preparative nucleophilic substitution by way of [2]-, [3]-, and [4]betylates. Stoichiometric phase transfer and substrate-reagent ion-pair (SRIP) reactions of betylates
2-Hydroxyethanesulphonyl chloride: a sulphonyl chloride with a primary hydroxy-group
作者:James F. King、John H. Hillhouse
DOI:10.1039/c39810000295
日期:——
The preparation of 2-hydroxyethanesulphonylchloride (1), the first example of compound containing both sulphonylchloride and primary alcohol functions, is described; reaction of (1) with base gives products evidently derived from the sulphene (4) and the β-sultone (6).
Alkylation of sulfonate anions via substrate-reagent ion-pair (srip) reactions of [2]betylates. Preparation of alkyl esters of hydroxyalkanesulfonic acids
作者:J.F. King、M. Aslam
DOI:10.1016/s0040-4039(01)81961-4
日期:1981.1
KING, J. F.;ASLAM, M., TETRAHEDRON LETT., 1981, 22, N 37, 3573-3576
作者:KING, J. F.、ASLAM, M.
DOI:——
日期:——
KING, J. F.;LOOSMORE, S. M.;ASLAM, M. LOCK, J. D.;MCGARRITY, M. J., J. AMER. CHEM. SOC., 1982, 104, N 25, 7108-7122
作者:KING, J. F.、LOOSMORE, S. M.、ASLAM, M. LOCK, J. D.、MCGARRITY, M. J.