Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles

Scott I. Bell; Steven M. Weinreb

doi:10.1016/S0040-4039(00)80462-1

Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles

Scott I. Bell, Steven M. Weinreb

Chemistry

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

12 Scopus citations

Abstract

Normally unreactive N-alkyl-N-sulfinyl compounds act as dienophiles in both inter and intramolecular Diels-Alder processes in the presence of Lewis acids or optimally under high pressure.

Original language	English (US)
Pages (from-to)	4233-4236
Number of pages	4
Journal	Tetrahedron Letters
Volume	29
Issue number	34
DOIs	https://doi.org/10.1016/S0040-4039(00)80462-1
State	Published - 1988

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)80462-1

Cite this

@article{358f1ac688c241f2bb10a203cfe1c459,

title = "Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles",

abstract = "Normally unreactive N-alkyl-N-sulfinyl compounds act as dienophiles in both inter and intramolecular Diels-Alder processes in the presence of Lewis acids or optimally under high pressure.",

author = "Bell, {Scott I.} and Weinreb, {Steven M.}",

note = "Funding Information: grateful to the National Science Foundation (CHE-84-02127) for support",

year = "1988",

doi = "10.1016/S0040-4039(00)80462-1",

language = "English (US)",

volume = "29",

pages = "4233--4236",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "34",

}

TY - JOUR

T1 - Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles

AU - Bell, Scott I.

AU - Weinreb, Steven M.

N1 - Funding Information: grateful to the National Science Foundation (CHE-84-02127) for support

PY - 1988

Y1 - 1988

N2 - Normally unreactive N-alkyl-N-sulfinyl compounds act as dienophiles in both inter and intramolecular Diels-Alder processes in the presence of Lewis acids or optimally under high pressure.

AB - Normally unreactive N-alkyl-N-sulfinyl compounds act as dienophiles in both inter and intramolecular Diels-Alder processes in the presence of Lewis acids or optimally under high pressure.

UR - http://www.scopus.com/inward/record.url?scp=0038597781&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0038597781&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)80462-1

DO - 10.1016/S0040-4039(00)80462-1

M3 - Article

AN - SCOPUS:0038597781

SN - 0040-4039

VL - 29

SP - 4233

EP - 4236

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 34

ER -

Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this