Satyanarayana, N.; Nayak, U. R., Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1985, vol. 24, p. 1107 - 1110
Studies in sesquiterpenes-lx reversion of longipinane to himachalane system : revision of structure of isocentdarol
作者:Mayank H Shastri、Sukh Dev
DOI:10.1016/s0040-4020(01)81583-0
日期:1992.6
Longipinene on exposure to acids rapidly rearranges to furnish α - and β-himachalenes, longifolene and isolongifolene. Longipinene epoxide, under acid catalysis, gives several products resulting from fragmentation and Wagner-Meerweinrearrangement. All products have been fully characterised. Formation of isocentdarol in this reaction requires revision of its stereochemistry at the centre carrying tertiary
Yadav, J. S.; Chawla, H. P. S.; Dev, Sukh, Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1983, vol. 22, # 3, p. 212 - 214
作者:Yadav, J. S.、Chawla, H. P. S.、Dev, Sukh
DOI:——
日期:——
Satyanarayana, N.; Nayak, U. R., Synthetic Communications, 1985, vol. 15, # 4, p. 331 - 334
作者:Satyanarayana, N.、Nayak, U. R.
DOI:——
日期:——
Satyanarayana, N.; Nayak, U. R., Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1985, vol. 24, p. 1107 - 1110