Enantioselective N-sulfinyl dienophile diels-alder cycloadditions

Stacy W. Remiszewski; Joongik Yang; Steven M. Weinreb

doi:10.1016/S0040-4039(00)84393-2

Enantioselective N-sulfinyl dienophile diels-alder cycloadditions

Stacy W. Remiszewski, Joongik Yang, Steven M. Weinreb

Chemistry

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

29 Scopus citations

Abstract

N-Sulfinyl carbamates prepared from phenylmenthol (1) and (+) -camphor- derived alcohol 10 display high enantioselectivity in TiCl₄ catalyzed [4+2] cycloadditions with 1,3-cyclohexadiene.

Original language	English (US)
Pages (from-to)	1853-1856
Number of pages	4
Journal	Tetrahedron Letters
Volume	27
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4039(00)84393-2
State	Published - 1986

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)84393-2

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@article{99854cc23bb34e30bdaceb870856184a,

title = "Enantioselective N-sulfinyl dienophile diels-alder cycloadditions",

abstract = "N-Sulfinyl carbamates prepared from phenylmenthol (1) and (+) -camphor- derived alcohol 10 display high enantioselectivity in TiCl4 catalyzed [4+2] cycloadditions with 1,3-cyclohexadiene.",

author = "Remiszewski, {Stacy W.} and Joongik Yang and Weinreb, {Steven M.}",

note = "Funding Information: We thank the National Science Foundation (CHE-84-02127)",

year = "1986",

doi = "10.1016/S0040-4039(00)84393-2",

language = "English (US)",

volume = "27",

pages = "1853--1856",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "17",

}

TY - JOUR

T1 - Enantioselective N-sulfinyl dienophile diels-alder cycloadditions

AU - Remiszewski, Stacy W.

AU - Yang, Joongik

AU - Weinreb, Steven M.

N1 - Funding Information: We thank the National Science Foundation (CHE-84-02127)

PY - 1986

Y1 - 1986

N2 - N-Sulfinyl carbamates prepared from phenylmenthol (1) and (+) -camphor- derived alcohol 10 display high enantioselectivity in TiCl4 catalyzed [4+2] cycloadditions with 1,3-cyclohexadiene.

AB - N-Sulfinyl carbamates prepared from phenylmenthol (1) and (+) -camphor- derived alcohol 10 display high enantioselectivity in TiCl4 catalyzed [4+2] cycloadditions with 1,3-cyclohexadiene.

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UR - http://www.scopus.com/inward/citedby.url?scp=0001681471&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)84393-2

DO - 10.1016/S0040-4039(00)84393-2

M3 - Article

AN - SCOPUS:0001681471

SN - 0040-4039

VL - 27

SP - 1853

EP - 1856

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

Enantioselective N-sulfinyl dienophile diels-alder cycloadditions

Abstract

All Science Journal Classification (ASJC) codes

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