Approaches to the synthesis of the lamellarins and related natural products. A review

被引：92

作者：

Handy, ST ^{[1
]}

Zhang, YN ^{[1
]}

机构：

[1] SUNY Binghamton, Dept Chem, Binghamton, NY 13902 USA

来源：

ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL | 2005年 / 37卷 / 05期

关键词：

D O I：

10.1080/00304940509354977

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：411 / +

页数：34

共 46 条

[1] METABOLITIES OF THE MARINE PROSOBRANCH MOLLUSK LAMELLARIA SP [J].

ANDERSEN, RJ ;

FAULKNER, DJ ;

HE, CH ;

VANDUYNE, GD ;

CLARDY, J .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (19) :5492-5495

[2]

Bach T, 1998, SYNLETT, P1185

[3]

Bach T, 1999, EUR J ORG CHEM, V1999, P2045

[4] Sequential Pd(0)-catalyzed reactions for the construction of multiple substituted furans.: A short synthesis of the F5 furan fatty acid [J].

Bach, T ;

Krüger, L .

TETRAHEDRON LETTERS, 1998, 39 (13) :1729-1732

[5] Convergent total synthesis of lamellarin K [J].

Banwell, M ;

Flynn, B ;

Hockless, D .

CHEMICAL COMMUNICATIONS, 1997, (23) :2259-2260

[6] Assessment of double-barrelled heck cyclizations as a means for construction of the 14-phenyl-8,9-dihydro-6H-[1]benzopyrano[4′,3′:4,5]pyrrolo[2,1-a]isoquinolin-6-one core associated with certain members of the lamellarin class of marine natural product [J].

Banwell, MG ;

Flynn, BL ;

Hockless, DCR ;

Longmore, RW ;

Rae, AD .

AUSTRALIAN JOURNAL OF CHEMISTRY, 1999, 52 (08) :755-765

[7] Convergent syntheses of the pyrrolic marine natural products lamellarin-O, lamellarin-Q, lukianol-A and some more highly oxygenated congeners [J].

Banwell, MG ;

Flynn, BL ;

Hamel, E ;

Hockless, DCR .

CHEMICAL COMMUNICATIONS, 1997, (02) :207-208

[8] Total synthesis of ningalin B utilizing a heterocyclic azadiene Diels-Alder reaction and discovery of a new class of potent multidrug resistant (MDR) reversal agents [J].

Boger, DL ;

Soenen, DR ;

Boyce, CW ;

Hedrick, MP ;

Jin, Q .

JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (08) :2479-2483

[9] Total syntheses of ningalin A, lamellarin O, lukianol A, and permethyl storniamide A utilizing heterocyclic azadiene Diels-Alder reactions [J].

Boger, DL ;

Boyce, CW ;

Labroli, MA ;

Sehon, CA ;

Jin, Q .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (01) :54-62

[10] STUDIES OF AUSTRALIAN ASCIDIANS .1. 6 NEW LAMELLARIN-CLASS ALKALOIDS FROM A COLONIAL ASCIDIAN, DIDEMNUM-SP [J].

CARROLL, AR ;

BOWDEN, BF ;

COLL, JC .

AUSTRALIAN JOURNAL OF CHEMISTRY, 1993, 46 (04) :489-501

← 1 2 3 4 5 →