A further synthesis of the corticosteroid side chain starting with a suitable 17-ketone

Research output: Contribution to journal › Article › peer-review

Abstract

The readily available olefin (8) is easily converted into the synthetically useful enamide (15) via the nitrosyl chloride adduct (9).

Original language	English
Pages (from-to)	2191-2192
Number of pages	2
Journal	Journal of the Chemical Society. Perkin Transactions 1
DOIs	https://doi.org/10.1039/p19850002191
Publication status	Published - 1 Jan 1985
Externally published	Yes

@article{cd050865db0640319bfbaf2d2268fb22,

title = "A further synthesis of the corticosteroid side chain starting with a suitable 17-ketone",

abstract = "The readily available olefin (8) is easily converted into the synthetically useful enamide (15) via the nitrosyl chloride adduct (9).",

author = "Barton, \{Derek H.R.\} and Zard, \{Samir Z.\}",

year = "1985",

month = jan,

day = "1",

doi = "10.1039/p19850002191",

language = "English",

pages = "2191--2192",

journal = "Journal of the Chemical Society. Perkin Transactions 1",

issn = "1472-7781",

}

TY - JOUR

T1 - A further synthesis of the corticosteroid side chain starting with a suitable 17-ketone

AU - Barton, Derek H.R.

AU - Zard, Samir Z.

PY - 1985/1/1

Y1 - 1985/1/1

N2 - The readily available olefin (8) is easily converted into the synthetically useful enamide (15) via the nitrosyl chloride adduct (9).

AB - The readily available olefin (8) is easily converted into the synthetically useful enamide (15) via the nitrosyl chloride adduct (9).

U2 - 10.1039/p19850002191

DO - 10.1039/p19850002191

M3 - Article

AN - SCOPUS:37049107898

SN - 1472-7781

SP - 2191

EP - 2192

JO - Journal of the Chemical Society. Perkin Transactions 1

JF - Journal of the Chemical Society. Perkin Transactions 1

ER -