Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin

Isao Kadota; Shioko Saya; Yoshinori Yamamoto

Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin

Isao Kadota, Shioko Saya, Yoshinori Yamamoto

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

Abstract

The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.

Original language	English
Pages (from-to)	335-348
Number of pages	14
Journal	Heterocycles
Volume	46
Issue number	1
Publication status	Published - Dec 1 1997
Externally published	Yes

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Fingerprint Dive into the research topics of 'Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin'. Together they form a unique fingerprint.

Cite this

@article{9c73f00a3d184035a3363231bd715945,

title = "Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin",

abstract = "The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.",

author = "Isao Kadota and Shioko Saya and Yoshinori Yamamoto",

year = "1997",

month = dec,

day = "1",

language = "English",

volume = "46",

pages = "335--348",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "1",

}

TY - JOUR

T1 - Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin

AU - Kadota, Isao

AU - Saya, Shioko

AU - Yamamoto, Yoshinori

PY - 1997/12/1

Y1 - 1997/12/1

N2 - The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.

AB - The thermal cyclization of γ-aminoallylstannane (8) having an aldehyde group gave β-hydroxypyrrolidine derivative (9a) as a sole product. This methodology was applied successfully to the total synthesis of (+)-preussin.

UR - http://www.scopus.com/inward/record.url?scp=0000391968&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0000391968&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0000391968

VL - 46

SP - 335

EP - 348

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

IS - 1

ER -

Novel route to the synthesis of hydroxylated pyrrolidine derivatives via the intramolecular reaction of γ-aminoallylstannane with aldehyde. Total synthesis of (+)-preussin

Abstract

ASJC Scopus subject areas

Other files and links

Cite this