β‐Angelica lactone epoxide: Chemical behaviour and some synthetic applications

R. M. Ortuño; J. Cardellach; J. Font

doi:10.1002/jhet.5570240117

β‐Angelica lactone epoxide: Chemical behaviour and some synthetic applications

R. M. Ortuño, J. Cardellach, J. Font

Department of Chemistry

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

26 Citations (Scopus)

Abstract

A new epoxy derivative of ß‐angelica lactone has been synthesized. Its chemical behaviour towards nucleophiles has been explored in order to prepare natural products with a trisubstituted ß‐hydroxy‐γ‐methylbutyrolactone‐type constitution. Thus, some potential precursors have been obtained and an efficient and stereo‐controlled synthesis of (±)‐blastmycinone is reported. Copyright © 1987 Journal of Heterocyclic Chemistry

Original language	English
Pages (from-to)	79-84
Journal	Journal of Heterocyclic Chemistry
Volume	24
Issue number	1
DOIs	https://doi.org/10.1002/jhet.5570240117
Publication status	Published - 1 Jan 1987

Access to Document

10.1002/jhet.5570240117

Cite this

@article{e69a0baf9c184b339a191bdd5dc6d41b,

title = "β‐Angelica lactone epoxide: Chemical behaviour and some synthetic applications",

abstract = "A new epoxy derivative of {\ss}‐angelica lactone has been synthesized. Its chemical behaviour towards nucleophiles has been explored in order to prepare natural products with a trisubstituted {\ss}‐hydroxy‐γ‐methylbutyrolactone‐type constitution. Thus, some potential precursors have been obtained and an efficient and stereo‐controlled synthesis of (±)‐blastmycinone is reported. Copyright {\textcopyright} 1987 Journal of Heterocyclic Chemistry",

author = "Ortu{\~n}o, \{R. M.\} and J. Cardellach and J. Font",

year = "1987",

month = jan,

day = "1",

doi = "10.1002/jhet.5570240117",

language = "English",

volume = "24",

pages = "79--84",

journal = "Journal of Heterocyclic Chemistry",

issn = "0022-152X",

publisher = "John Wiley and Sons Inc.",

number = "1",

}

TY - JOUR

T1 - β‐Angelica lactone epoxide: Chemical behaviour and some synthetic applications

AU - Ortuño, R. M.

AU - Cardellach, J.

AU - Font, J.

PY - 1987/1/1

Y1 - 1987/1/1

N2 - A new epoxy derivative of ß‐angelica lactone has been synthesized. Its chemical behaviour towards nucleophiles has been explored in order to prepare natural products with a trisubstituted ß‐hydroxy‐γ‐methylbutyrolactone‐type constitution. Thus, some potential precursors have been obtained and an efficient and stereo‐controlled synthesis of (±)‐blastmycinone is reported. Copyright © 1987 Journal of Heterocyclic Chemistry

AB - A new epoxy derivative of ß‐angelica lactone has been synthesized. Its chemical behaviour towards nucleophiles has been explored in order to prepare natural products with a trisubstituted ß‐hydroxy‐γ‐methylbutyrolactone‐type constitution. Thus, some potential precursors have been obtained and an efficient and stereo‐controlled synthesis of (±)‐blastmycinone is reported. Copyright © 1987 Journal of Heterocyclic Chemistry

UR - https://www.scopus.com/pages/publications/0002445318

U2 - 10.1002/jhet.5570240117

DO - 10.1002/jhet.5570240117

M3 - Article

SN - 0022-152X

VL - 24

SP - 79

EP - 84

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 1

ER -

β‐Angelica lactone epoxide: Chemical behaviour and some synthetic applications

Abstract

Access to Document

Other files and links

Fingerprint

Cite this