STEREOSELECTIVE SYNTHESIS OF A 13-AZAPROSTACYCLIN METHYL-ESTER

被引：8

作者：

COLLINGTON, EW

FINCH, H

WALLIS, CJ

机构：

来源：

TETRAHEDRON LETTERS | 1983年 / 24卷 / 30期

关键词：

D O I：

10.1016/S0040-4039(00)88112-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3121 / 3124

页数：4

共 11 条

[1]

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[3]

BRADBURY RH, 1982, TETRAHEDRON LETT, V23, P1335

[4]

BUNDY GL, 1978, TETRAHEDRON LETT, V19, P1371

[5]

GALAMBOS G, 1977, TETRAHEDRON LETT, V18, P2627

[6]

GALAMBOS G, 1978, TETRAHEDRON LETT, V19, P581

[7] 6,9-THIAPROSTACYCLIN - STABLE AND BIOLOGICALLY POTENT ANALOG OF PROSTACYCLIN (PGI2) [J].

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BARNETTE, WE ;

GASIC, GP ;

MAGOLDA, RL .

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[8] TOTAL SYNTHESIS OF CARBOPROSTACYCLIN, A STABLE AND BIOLOGICALLY-ACTIVE ANALOG OF PROSTACYCLIN (PGI2) [J].

NICOLAOU, KC ;

SIPIO, WJ ;

MAGOLDA, RL ;

SEITZ, S ;

BARNETTE, WE .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (23) :1067-1068

[9] SYNTHESE OF 13-OXA-PGI AND 13-THIA-PGI2 - METABOLICALLY STABLE AND BIOLOGICALLY POTENT PGI2 ANALOGS [J].

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ASZODI, J ;

SZANTAY, C .

TETRAHEDRON LETTERS, 1982, 23 (20) :2135-2138

[10] REARRANGEMENTS OF BICYCLO[3,2,0]HEPTAN-6-ONES - SYNTHESIS OF POTENTIAL PROSTANOID PRECURSORS [J].

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