Intramolecular cycloaddition of 3-O-cyclohexenyl carbohydrate nitrones: Diastereoselective synthesis of optically pure tetrahydropyrano[2,3]cyclohexane derivatives

被引：5

作者：

Bhattacharjee, A

Bhattacharjya, A

Patra, A

机构：

[1] INDIAN INST CHEM BIOL,CALCUTTA 700032,W BENGAL,INDIA

[2] UNIV CALCUTTA,UNIV COLL SCI,DEPT CHEM,CTR ADV STUDIES NAT PROD,CALCUTTA 700009,W BENGAL,INDIA

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 42期

关键词：

D O I：

10.1016/0040-4039(96)01680-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The intramolecular cycloaddition of nitrones derived from 3-O-cyclohexenylfuranoside-5-aldehydes led to diastereoselective formation of tetrahydropyrano[2, 3]cyclohexane ring systems with six chiral centres. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：7635 / 7636

页数：2

共 3 条

[1] Formation of non-racemic tricyclic compounds by intramolecular 1,3-dipolar cycloaddition of nitrones [J].

Aurich, HG ;

Geiger, M ;

Gentes, C ;

Koster, H .

TETRAHEDRON LETTERS, 1996, 37 (06) :841-844

[2] SYNTHESIS OF ENANTIOMERIC PYRANS FROM A 3-O-ALLYLALLOSE DERIVATIVE BY THE APPLICATION OF INTRAMOLECULAR NITRONE CYCLOADDITION [J].

BHATTACHARJEE, A ;

BHATTACHARJYA, A ;

PATRA, A .

TETRAHEDRON LETTERS, 1995, 36 (26) :4677-4680

[3] SYNTHESIS OF OPTICALLY PURE TETRAHYDROFURANS FROM 2-(O)UNDER-BAR-ALLYLGLUCOSE DERIVATIVES BY INTRAMOLECULAR NITRONE CYCLOADDITION - PREFERENTIAL FORMATION OF A FURANOISOXAZOLIDINE FROM PENTA-(O)UNDER-BAR-ALLYLGLUCOSE [J].

MUKHOPADHYAY, R ;

KUNDU, AP ;

BHATTACHARJYA, A .

TETRAHEDRON LETTERS, 1995, 36 (42) :7729-7730

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