Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction

Katsuhiko Tomooka; Tatsuyuki Okinaga; Keisuke Suzuki; Gen ichi Tsuchihashi

doi:10.1016/S0040-4039(01)91367-X

Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction

Katsuhiko Tomooka, Tatsuyuki Okinaga, Keisuke Suzuki, Gen ichi Tsuchihashi

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

48 Citations (Scopus)

Abstract

Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.

Original language	English
Pages (from-to)	6335-6338
Number of pages	4
Journal	Tetrahedron Letters
Volume	28
Issue number	50
DOIs	https://doi.org/10.1016/S0040-4039(01)91367-X
Publication status	Published - 1987
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(01)91367-X

Cite this

@article{614dbe503cc24d6294f27977dbdf54ee,

title = "Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction",

abstract = "Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.",

author = "Katsuhiko Tomooka and Tatsuyuki Okinaga and Keisuke Suzuki and Tsuchihashi, {Gen ichi}",

year = "1987",

doi = "10.1016/S0040-4039(01)91367-X",

language = "English",

volume = "28",

pages = "6335--6338",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "50",

}

TY - JOUR

T1 - Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction

AU - Tomooka, Katsuhiko

AU - Okinaga, Tatsuyuki

AU - Suzuki, Keisuke

AU - Tsuchihashi, Gen ichi

PY - 1987

Y1 - 1987

N2 - Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.

AB - Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.

UR - http://www.scopus.com/inward/record.url?scp=0000606901&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0000606901&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(01)91367-X

DO - 10.1016/S0040-4039(01)91367-X

M3 - Article

AN - SCOPUS:0000606901

VL - 28

SP - 6335

EP - 6338

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 50

ER -

Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this