Palladium(II)-catalyzed synthesis of isoxazolidines: Using a catalytic copper acetate and molecular oxygen as the cooxidant

Krishna Gopal Dongol; Ying Tay Boon; Kai Xiang; Thies Thiemann

doi:10.1080/00397910500516233

Palladium(II)-catalyzed synthesis of isoxazolidines: Using a catalytic copper acetate and molecular oxygen as the cooxidant

Krishna Gopal Dongol
, Ying Tay Boon
, Kai Xiang
, Thies Thiemann

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

12 Citations (Scopus)

Abstract

An environmentally friendly process is reported for the palladium(II)-catalyzed cyclofunctionalization of allylic hydroxylamine derivatives using a catalytic amount of copper(II) acetate and molecular oxygen as the cooxidant.

Original language	English
Pages (from-to)	1247-1257
Number of pages	11
Journal	Synthetic Communications
Volume	36
Issue number	9
DOIs	https://doi.org/10.1080/00397910500516233
Publication status	Published - 2006
Externally published	Yes

Keywords

Allyl hydroxylamine
Cyclofunctionalization
Isoxazolidine
Molecular oxygen
Palladium(II) catalysis

ASJC Scopus subject areas

Organic Chemistry

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10.1080/00397910500516233

Cite this

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title = "Palladium(II)-catalyzed synthesis of isoxazolidines: Using a catalytic copper acetate and molecular oxygen as the cooxidant",

abstract = "An environmentally friendly process is reported for the palladium(II)-catalyzed cyclofunctionalization of allylic hydroxylamine derivatives using a catalytic amount of copper(II) acetate and molecular oxygen as the cooxidant.",

keywords = "Allyl hydroxylamine, Cyclofunctionalization, Isoxazolidine, Molecular oxygen, Palladium(II) catalysis",

author = "Dongol, \{Krishna Gopal\} and Boon, \{Ying Tay\} and Kai Xiang and Thies Thiemann",

note = "Funding Information: Authors thank the Agency for Science, Technology, and Research (A*STAR) of Singapore under project code ICES 03-142001 for financial support. The authors also thank Holger Butenschoen, University of Hannover, Germany, for giving valuable suggestions and comments for this manuscript. The authors are very grateful to Felicity Kate Moore for correcting the manuscript.",

year = "2006",

doi = "10.1080/00397910500516233",

language = "English",

volume = "36",

pages = "1247--1257",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor and Francis Ltd.",

number = "9",

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TY - JOUR

T1 - Palladium(II)-catalyzed synthesis of isoxazolidines

T2 - Using a catalytic copper acetate and molecular oxygen as the cooxidant

AU - Dongol, Krishna Gopal

AU - Boon, Ying Tay

AU - Xiang, Kai

AU - Thiemann, Thies

N1 - Funding Information: Authors thank the Agency for Science, Technology, and Research (A*STAR) of Singapore under project code ICES 03-142001 for financial support. The authors also thank Holger Butenschoen, University of Hannover, Germany, for giving valuable suggestions and comments for this manuscript. The authors are very grateful to Felicity Kate Moore for correcting the manuscript.

PY - 2006

Y1 - 2006

N2 - An environmentally friendly process is reported for the palladium(II)-catalyzed cyclofunctionalization of allylic hydroxylamine derivatives using a catalytic amount of copper(II) acetate and molecular oxygen as the cooxidant.

AB - An environmentally friendly process is reported for the palladium(II)-catalyzed cyclofunctionalization of allylic hydroxylamine derivatives using a catalytic amount of copper(II) acetate and molecular oxygen as the cooxidant.

KW - Allyl hydroxylamine

KW - Cyclofunctionalization

KW - Isoxazolidine

KW - Molecular oxygen

KW - Palladium(II) catalysis

UR - https://www.scopus.com/pages/publications/33645291224

UR - https://www.scopus.com/pages/publications/33645291224#tab=citedBy

U2 - 10.1080/00397910500516233

DO - 10.1080/00397910500516233

M3 - Article

AN - SCOPUS:33645291224

SN - 0039-7911

VL - 36

SP - 1247

EP - 1257

JO - Synthetic Communications

JF - Synthetic Communications

IS - 9

ER -

Palladium(II)-catalyzed synthesis of isoxazolidines: Using a catalytic copper acetate and molecular oxygen as the cooxidant

Abstract

Keywords

ASJC Scopus subject areas

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