Synthesis of 7-methoxybenzolactam-V8 using a diastereoselective Strecker synthesis

S. Sakamuri; A. P. Kozikowski

doi:10.1039/b008970m

Synthesis of 7-methoxybenzolactam-V8 using a diastereoselective Strecker synthesis

S. Sakamuri, A. P. Kozikowski

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

9 Scopus citations

Abstract

7-Methoxybenzolactam-V8 (4) was synthesized using a diastereoselective Strecker reaction as the key step employing an ortho-substituted phenylacetaldehyde and (R)-phenylglycinol as the chiral auxiliary.

Original language	English (US)
Pages (from-to)	475-476
Number of pages	2
Journal	Chemical Communications
Issue number	5
DOIs	https://doi.org/10.1039/b008970m
State	Published - Mar 7 2001
Externally published	Yes

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/b008970m

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@article{edc6d089016242d9999963ff39bf3e72,

title = "Synthesis of 7-methoxybenzolactam-V8 using a diastereoselective Strecker synthesis",

abstract = "7-Methoxybenzolactam-V8 (4) was synthesized using a diastereoselective Strecker reaction as the key step employing an ortho-substituted phenylacetaldehyde and (R)-phenylglycinol as the chiral auxiliary.",

author = "S. Sakamuri and Kozikowski, {A. P.}",

year = "2001",

month = mar,

day = "7",

doi = "10.1039/b008970m",

language = "English (US)",

pages = "475--476",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "5",

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T1 - Synthesis of 7-methoxybenzolactam-V8 using a diastereoselective Strecker synthesis

AU - Sakamuri, S.

AU - Kozikowski, A. P.

PY - 2001/3/7

Y1 - 2001/3/7

N2 - 7-Methoxybenzolactam-V8 (4) was synthesized using a diastereoselective Strecker reaction as the key step employing an ortho-substituted phenylacetaldehyde and (R)-phenylglycinol as the chiral auxiliary.

AB - 7-Methoxybenzolactam-V8 (4) was synthesized using a diastereoselective Strecker reaction as the key step employing an ortho-substituted phenylacetaldehyde and (R)-phenylglycinol as the chiral auxiliary.

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UR - http://www.scopus.com/inward/citedby.url?scp=0035819969&partnerID=8YFLogxK

U2 - 10.1039/b008970m

DO - 10.1039/b008970m

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AN - SCOPUS:0035819969

SN - 1359-7345

SP - 475

EP - 476

JO - Chemical Communications

JF - Chemical Communications

IS - 5

ER -

Synthesis of 7-methoxybenzolactam-V8 using a diastereoselective Strecker synthesis

Abstract

ASJC Scopus subject areas

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