A concise synthesis of a potential key intermediate for 12-epi-mycalamide A

Marcellino Rudyanto; Masahiro Toyota; Natsuko Kagawa; Masataka Ihara

A concise synthesis of a potential key intermediate for 12-epi-mycalamide A

Marcellino Rudyanto, Masahiro Toyota, Natsuko Kagawa, Masataka Ihara

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

3 Citations (Scopus)

Abstract

Intramolecular nitrile oxide cycloaddition (INOC) reaction of the oximes (7) provides the isoxazoline (9), a possible key intermediate for 12-epi-mycalamide A (2).

Original language	English
Pages (from-to)	655-658
Number of pages	4
Journal	Heterocycles
Volume	58
Publication status	Published - 22 Nov 2002
Externally published	Yes

Cite this

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title = "A concise synthesis of a potential key intermediate for 12-epi-mycalamide A",

abstract = "Intramolecular nitrile oxide cycloaddition (INOC) reaction of the oximes (7) provides the isoxazoline (9), a possible key intermediate for 12-epi-mycalamide A (2).",

author = "Marcellino Rudyanto and Masahiro Toyota and Natsuko Kagawa and Masataka Ihara",

year = "2002",

month = nov,

day = "22",

language = "English",

volume = "58",

pages = "655--658",

journal = "Heterocycles",

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publisher = "Japan Institute of Heterocyclic Chemistry",

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T1 - A concise synthesis of a potential key intermediate for 12-epi-mycalamide A

AU - Rudyanto, Marcellino

AU - Toyota, Masahiro

AU - Kagawa, Natsuko

AU - Ihara, Masataka

PY - 2002/11/22

Y1 - 2002/11/22

N2 - Intramolecular nitrile oxide cycloaddition (INOC) reaction of the oximes (7) provides the isoxazoline (9), a possible key intermediate for 12-epi-mycalamide A (2).

AB - Intramolecular nitrile oxide cycloaddition (INOC) reaction of the oximes (7) provides the isoxazoline (9), a possible key intermediate for 12-epi-mycalamide A (2).

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M3 - Article

AN - SCOPUS:0037159705

SN - 0385-5414

VL - 58

SP - 655

EP - 658

JO - Heterocycles

JF - Heterocycles

ER -

A concise synthesis of a potential key intermediate for 12-epi-mycalamide A

Abstract

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