Synthesis of novel chiral bisazetidines by the hydroalane reduction of bis-beta-lactams

Iwao Ojima; Takehiko Yamato; Kazuaki Nakahashi

doi:10.1016/S0040-4039(00)94772-5

Synthesis of novel chiral bisazetidines by the hydroalane reduction of bis-beta-lactams

Iwao Ojima
, Takehiko Yamato
, Kazuaki Nakahashi

Chemistry

Stony Brook University

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

Abstract

A series of novel chiral bisazetidines in which two azetidine rings are either directly connected or coupled in tandem style, are synthesized in good yields by the hydroalane reduction of the corresponding bis-beta-lactame.

Original language	English
Pages (from-to)	2035-2038
Number of pages	4
Journal	Tetrahedron Letters
Volume	26
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4039(00)94772-5
State	Published - 1985

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@article{fc0a7de5338d468c92c3aebb490eb599,

title = "Synthesis of novel chiral bisazetidines by the hydroalane reduction of bis-beta-lactams",

abstract = "A series of novel chiral bisazetidines in which two azetidine rings are either directly connected or coupled in tandem style, are synthesized in good yields by the hydroalane reduction of the corresponding bis-beta-lactame.",

author = "Iwao Ojima and Takehiko Yamato and Kazuaki Nakahashi",

year = "1985",

doi = "10.1016/S0040-4039(00)94772-5",

language = "English",

volume = "26",

pages = "2035--2038",

journal = "Tetrahedron Letters",

issn = "0040-4039",

number = "17",

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TY - JOUR

T1 - Synthesis of novel chiral bisazetidines by the hydroalane reduction of bis-beta-lactams

AU - Ojima, Iwao

AU - Yamato, Takehiko

AU - Nakahashi, Kazuaki

PY - 1985

Y1 - 1985

N2 - A series of novel chiral bisazetidines in which two azetidine rings are either directly connected or coupled in tandem style, are synthesized in good yields by the hydroalane reduction of the corresponding bis-beta-lactame.

AB - A series of novel chiral bisazetidines in which two azetidine rings are either directly connected or coupled in tandem style, are synthesized in good yields by the hydroalane reduction of the corresponding bis-beta-lactame.

UR - https://www.scopus.com/pages/publications/0021958593

U2 - 10.1016/S0040-4039(00)94772-5

DO - 10.1016/S0040-4039(00)94772-5

M3 - Article

AN - SCOPUS:0021958593

SN - 0040-4039

VL - 26

SP - 2035

EP - 2038

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

Synthesis of novel chiral bisazetidines by the hydroalane reduction of bis-beta-lactams

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