Asymmetric synthesis of cis-aminochromanol

Karl B. Hansen; Philippe Rabbat; Shawn A. Springfield; Paul N. Devine; Edward J.J. Grabowski; Paul J. Reider

doi:10.1016/S0040-4039(01)01907-4

Asymmetric synthesis of cis-aminochromanol

Karl B. Hansen
, Philippe Rabbat
, Shawn A. Springfield
, Paul N. Devine
, Edward J.J. Grabowski
, Paul J. Reider

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

18 Scopus citations

Abstract

An efficient asymmetric synthesis of cis-aminochromanol was achieved in seven steps. The absolute stereochemistry of cis-aminochromanol was derived from (salen)Co(III)-catalyzed phenol opening of methyl glycidate.

Original language	English (US)
Pages (from-to)	8743-8745
Number of pages	3
Journal	Tetrahedron Letters
Volume	42
Issue number	50
DOIs	https://doi.org/10.1016/S0040-4039(01)01907-4
State	Published - Dec 10 2001
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)01907-4

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@article{0bccfa47f15e4232bcd38f4c35ce2a20,

title = "Asymmetric synthesis of cis-aminochromanol",

abstract = "An efficient asymmetric synthesis of cis-aminochromanol was achieved in seven steps. The absolute stereochemistry of cis-aminochromanol was derived from (salen)Co(III)-catalyzed phenol opening of methyl glycidate.",

author = "Hansen, \{Karl B.\} and Philippe Rabbat and Springfield, \{Shawn A.\} and Devine, \{Paul N.\} and Grabowski, \{Edward J.J.\} and Reider, \{Paul J.\}",

year = "2001",

month = dec,

day = "10",

doi = "10.1016/S0040-4039(01)01907-4",

language = "English (US)",

volume = "42",

pages = "8743--8745",

journal = "Tetrahedron Letters",

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number = "50",

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T1 - Asymmetric synthesis of cis-aminochromanol

AU - Hansen, Karl B.

AU - Rabbat, Philippe

AU - Springfield, Shawn A.

AU - Devine, Paul N.

AU - Grabowski, Edward J.J.

AU - Reider, Paul J.

PY - 2001/12/10

Y1 - 2001/12/10

N2 - An efficient asymmetric synthesis of cis-aminochromanol was achieved in seven steps. The absolute stereochemistry of cis-aminochromanol was derived from (salen)Co(III)-catalyzed phenol opening of methyl glycidate.

AB - An efficient asymmetric synthesis of cis-aminochromanol was achieved in seven steps. The absolute stereochemistry of cis-aminochromanol was derived from (salen)Co(III)-catalyzed phenol opening of methyl glycidate.

UR - https://www.scopus.com/pages/publications/0035842127

UR - https://www.scopus.com/pages/publications/0035842127#tab=citedBy

U2 - 10.1016/S0040-4039(01)01907-4

DO - 10.1016/S0040-4039(01)01907-4

M3 - Article

AN - SCOPUS:0035842127

SN - 0040-4039

VL - 42

SP - 8743

EP - 8745

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 50

ER -

Asymmetric synthesis of cis-aminochromanol

Abstract

All Science Journal Classification (ASJC) codes

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