COMPLEX PYRROLIDINES VIA A TANDEM MICHAEL REACTION/1,3-DIPOLAR CYCLOADDITION SEQUENCE - A NOVEL METHOD FOR THE GENERATION OF UNSYMMETRICAL AZOMETHINE YLIDES

被引：19

作者：

GARNER, P

ARYA, F

HO, WB

机构：

[1] Department of Chemistry, Case Western Reserve University, Cleveland

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1990年 / 55卷 / 02期

关键词：

D O I：

10.1021/jo00289a005

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A novel tandem Michael addition/1,3-dipolar cycloadditionprotocol for the assembly of the 3,8-diazabicyclo[3.2.1]octane ring system found in naphthyridino-mycin (7) and quinocarcin (2) is described. © 1990, American Chemical Society. All rights reserved.

引用

页码：412 / 414

页数：3

共 14 条

[1] CYCLOADDITION REACTIONS OF OXIMES - POWERFUL NEW CARBON CARBON BOND FORMING METHODOLOGY
ARMSTRONG, P
GRIGG, R
WARNOCK, WJ
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (17) : 1325 - 1327
[2] ASHER V, 1981, TETRAHEDRON LETT, P141
[3] COOK AG, 1969, ENAMINES SYNTHESIS S, P211
[4] AN ASYMMETRIC APPROACH TO NAPHTHYRIDINOMYCIN AND QUINOCARCIN VIA A REMARKABLY SELECTIVE INTRAMOLECULAR 1,3-DIPOLAR CYCLO-ADDITION REACTION
GARNER, P
SUNITHA, K
HO, WB
YOUNGS, WJ
KENNEDY, VO
DJEBLI, A
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (09) : 2041 - 2042
[5] AN APPROACH TO THE 3,8-DIAZABICYCLO[3.2.1]OCTANE MOIETY OF NAPHTHYRIDINOMYCIN AND QUINOCARCIN VIA 1,3-DIPOLAR CYCLO-ADDITION OF PHOTOCHEMICALLY GENERATED AZOMETHINE YLIDES
GARNER, P
SUNITHA, K
SHANTHILAL, T
[J]. TETRAHEDRON LETTERS, 1988, 29 (29) : 3525 - 3528
[6] TANDEM 1,3-DIPOLAR CYCLO-ADDITIONS OF PYRIDINIUM OR ISOQUINOLINIUM METHYLIDES WITH OLEFINIC DIPOLAROPHILES LEADING TO CYCL[3.2.2]AZINES - ENAMINE ROUTE AS A NEW GENERATION METHOD OF AZOMETHINE YLIDES
KANEMASA, S
TAKENAKA, S
WATANABE, H
TSUGE, O
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (02) : 420 - 424
[7] 1,3-DIPOLAR CYCLOADDITIONS TO OXIDOPYRAZINIUMS
KISS, M
RUSSELLMAYNARD, J
JOULE, JA
[J]. TETRAHEDRON LETTERS, 1987, 28 (19) : 2187 - 2190
[8] MASSA S, 1988, TETRAHEDRON LETT, P6471
[9] MENACHERY MD, 1983, TETRAHEDRON LETT, P167
[10] Pearson W. H., 1998, STUDIES NATURAL PROD, V1, P323

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