High-field NMR studies of 3β-tetrahydropyranyloxy steroids
摘要:
Comprehensive NMR studies were carried out on 3 beta-hydroxy-pregnene and cholestene analogs, each containing a tetrahydropyranyl ether group at the 3-position. Two-dimensional NMR experiments (COSY, TOCSY, HSQC, and HSQC-TOCSY) permitted the complete assignments of both the (1)H and (13)C resonances of these derivatives in deuterated benzene or chloroform. The aromatic solvent-induced NMR signal shifts (ASIS) were also investigated. (C) 2000 Elsevier Science Inc. All rights reserved.
High-field NMR studies of 3β-tetrahydropyranyloxy steroids
作者:Z Szendi
DOI:10.1016/s0039-128x(00)00103-3
日期:2000.7
Comprehensive NMR studies were carried out on 3 beta-hydroxy-pregnene and cholestene analogs, each containing a tetrahydropyranyl ether group at the 3-position. Two-dimensional NMR experiments (COSY, TOCSY, HSQC, and HSQC-TOCSY) permitted the complete assignments of both the (1)H and (13)C resonances of these derivatives in deuterated benzene or chloroform. The aromatic solvent-induced NMR signal shifts (ASIS) were also investigated. (C) 2000 Elsevier Science Inc. All rights reserved.