CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL

LANGER K, Mattay J, HEIDBREDER A, MOLLER M (1992)
Liebigs Annalen der Chemie (3): 257-260.

Journal Article | Published | German

No fulltext has been uploaded

Author
; ; ;
Abstract
Grandisol (10) is stereoselectively synthesized in 9 steps, starting from commercially available 3-methyl-3-buten-1-ol (1). The key step of the synthesis is the Cu(I)-catalyzed [2 + 2]-photocycloaddition of 3 to 4a or 4b. Moreover, solvent effects on the endo/exo product ratio of the [2 + 2]-photocycloaddition are investigated.
Publishing Year
ISSN
PUB-ID

Cite this

LANGER K, Mattay J, HEIDBREDER A, MOLLER M. CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL. Liebigs Annalen der Chemie. 1992;(3):257-260.
LANGER, K., Mattay, J., HEIDBREDER, A., & MOLLER, M. (1992). CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL. Liebigs Annalen der Chemie(3), 257-260.
LANGER, K., Mattay, J., HEIDBREDER, A., and MOLLER, M. (1992). CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL. Liebigs Annalen der Chemie, 257-260.
LANGER, K., et al., 1992. CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL. Liebigs Annalen der Chemie, (3), p 257-260.
K. LANGER, et al., “CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL”, Liebigs Annalen der Chemie, 1992, pp. 257-260.
LANGER, K., Mattay, J., HEIDBREDER, A., MOLLER, M.: CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL. Liebigs Annalen der Chemie. 257-260 (1992).
LANGER, K, Mattay, Jochen, HEIDBREDER, A, and MOLLER, M. “CYCLOADDITIONS .36. A NEW STEREOSELECTIVE SYNTHESIS OF GRANDISOL”. Liebigs Annalen der Chemie 3 (1992): 257-260.
This data publication is cited in the following publications:
This publication cites the following data publications:

Export

0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®

Search this title in

Google Scholar