One-pot three-component metathesis/Diels-Alder tandem reaction

被引：94

作者：

Lee, HY ^{[1
]}

Kim, HY

Tae, H

Kim, BG

Lee, J

机构：

[1] Korea Adv Inst Sci & Technol, Ctr Mol Design & Synth, Dept Chem, Taejon 305701, South Korea

[2] Korea Adv Inst Sci & Technol, Sch Mol Sci BK21, Taejon 305701, South Korea

来源：

ORGANIC LETTERS | 2003年 / 5卷 / 19期

关键词：

D O I：

10.1021/ol035194c

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A tandem enyne, diene-ene metathesis reaction followed by Diels-Alder reaction accomplished a stereoselective three-component reaction protocol with four stereocenters.

引用

页码：3439 / 3442

页数：4

共 39 条

[1]

[Anonymous], 1994, The G-Protein linked Receptor Fact Book

[2]

Armstrong SK, 1998, J CHEM SOC PERK T 1, P371

[3] Synthesis of ansa-bridged macrocyclic lactams related to the antitumor antibiotic geldanamycin by ring closing metathesis [J].

Bach, T ;

Lemarchand, A .

SYNLETT, 2002, (08) :1302-1304

[4] Totally atom economical tandem-metathesis and Diels-Alder approach to polycyclic compounds [J].

Banti, D ;

North, M .

TETRAHEDRON LETTERS, 2002, 43 (08) :1561-1564

[5]

Bentz D, 2000, SYNTHESIS-STUTTGART, P1766

[6] Design and synthesis of a piperazinylalkylisoxazole library for subtype selective dopamine receptor ligands [J].

Cha, MY ;

Choi, BC ;

Kang, KH ;

Pae, AN ;

Choi, KI ;

Cho, YS ;

Koh, HY ;

Lee, HY ;

Jung, D ;

Kong, JY .

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (10) :1327-1330

[7]

Dvorak CA, 2000, ANGEW CHEM INT EDIT, V39, P1664, DOI 10.1002/(SICI)1521-3773(20000502)39:9<1664::AID-ANIE1664>3.0.CO

[8]

2-#

[9] Design, Synthesis, and Application of Peptide Secondary Structure Mimetics [J].

Eguchi, Masakatsu ;

Kahn, Michael .

MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2002, 2 (05) :447-462

[10]

Fürstner A, 2000, ANGEW CHEM INT EDIT, V39, P3012

← 1 2 3 4 →