๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

An enantiospecific synthesis of estrone

โœ Scribed by John H. Hutchinson; Thomas Money

Book ID
104226736
Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
234 KB
Volume
26
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis

Efficient ring cleavage of 9,10-dibromocamphor (3) provides a monocyclic hydroxyacid (5) which can serve as an intermediate in a new enantiospecific synthesis of estrone.

๐Ÿ“œ SIMILAR VOLUMES

An Enantiospecific Synthesis of Jiadifen
An Enantiospecific Synthesis of Jiadifenolide
โœ Siler, David A.; Mighion, Jeffrey D.; Sorensen, Erik J. ๐Ÿ“‚ Article ๐Ÿ“… 2014 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 647 KB
An expeditious synthesis of estrone
An expeditious synthesis of estrone
โœ S. Danishefsky; P. Cain ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 493 KB
An Enantiospecific Synthesis of 2-Pupuke
An Enantiospecific Synthesis of 2-Pupukeanone.
โœ A. Srikrishna; P. Ravi Kumar; S. J. Gharpure ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons โš– 27 KB ๐Ÿ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Enantiospecific synthesis of an indolizi
Enantiospecific synthesis of an indolizidine alkaloid, (+)-ipalbidine
โœ Toshio Honda; Hidenori Namiki; Hiromasa Nagase; Hirotake Mizutani ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 179 KB

Enantiospecific total synthesis of an indolizidine alkaloid, ipalbidine, was achieved starting from (-)-pyroglutamic acid by employing an intramolecular McMurry coupling reaction with a low-valent titanium, as a key step.