Extension of the nenitzescu reaction to simple ketones provides an efficient route to 1'-alkyl-5'-hydroxynaltrindole analogues, potent and selective δ-opioid receptor antagonists

[No Value] Shefali, S K Srivastava, S M Husbands, J W Lewis

Research output: Contribution to journalArticle

14 Citations (Scopus)
Original languageEnglish
Pages (from-to)635-638
Number of pages4
JournalJournal of Medicinal Chemistry
Volume48
Publication statusPublished - 2005

Cite this

@article{53c97fd3ef304e50b4fb5bfc4126ac85,
title = "Extension of the nenitzescu reaction to simple ketones provides an efficient route to 1'-alkyl-5'-hydroxynaltrindole analogues, potent and selective δ-opioid receptor antagonists",
author = "Shefali, {[No Value]} and Srivastava, {S K} and Husbands, {S M} and Lewis, {J W}",
year = "2005",
language = "English",
volume = "48",
pages = "635--638",
journal = "Journal of Medicinal Chemistry",
issn = "0022-2623",
publisher = "American Chemical Society",

}

TY - JOUR

T1 - Extension of the nenitzescu reaction to simple ketones provides an efficient route to 1'-alkyl-5'-hydroxynaltrindole analogues, potent and selective δ-opioid receptor antagonists

AU - Shefali, [No Value]

AU - Srivastava, S K

AU - Husbands, S M

AU - Lewis, J W

PY - 2005

Y1 - 2005

M3 - Article

VL - 48

SP - 635

EP - 638

JO - Journal of Medicinal Chemistry

JF - Journal of Medicinal Chemistry

SN - 0022-2623

ER -