A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities

VK Aggarwal; E Alonso; I Bae; G Hynd; KM Lydon; MJ Palmer; M Patel; M Porcelloni; J Richardson; R Stenson; JR Studley; J-LCN Vasse; CL Winn

doi:10.1021/ja034606+

A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities

VK Aggarwal, E Alonso, I Bae, G Hynd, KM Lydon, MJ Palmer, M Patel, M Porcelloni, J Richardson, R Stenson, JR Studley, J-LCN Vasse, CL Winn

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

188 Citations (Scopus)

Translated title of the contribution	A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities
Original language	English
Pages (from-to)	10926 - 10940
Number of pages	15
Journal	Journal of the American Chemical Society
Volume	125 (36)
DOIs	https://doi.org/10.1021/ja034606+
Publication status	Published - Sept 2003

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Publisher: American Chemical Society

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10.1021/ja034606+

http://pubs.acs.org/cgi-bin/abstract.cgi/jacsat/2003/125/i36/abs/ja034606+.html

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Aggarwal, VK., Alonso, E., Bae, I., Hynd, G., Lydon, KM., Palmer, MJ., Patel, M., Porcelloni, M., Richardson, J., Stenson, R., Studley, JR., Vasse, J.-LCN., & Winn, CL. (2003). A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities. Journal of the American Chemical Society, 125 (36), 10926 - 10940. https://doi.org/10.1021/ja034606+

Aggarwal, VK ; Alonso, E ; Bae, I et al. / A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities. In: Journal of the American Chemical Society. 2003 ; Vol. 125 (36). pp. 10926 - 10940.

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title = "A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities",

author = "VK Aggarwal and E Alonso and I Bae and G Hynd and KM Lydon and MJ Palmer and M Patel and M Porcelloni and J Richardson and R Stenson and JR Studley and J-LCN Vasse and CL Winn",

note = "Publisher: American Chemical Society",

year = "2003",

month = sep,

doi = "10.1021/ja034606+",

language = "English",

volume = "125 (36)",

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journal = "Journal of the American Chemical Society",

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Aggarwal, VK, Alonso, E, Bae, I, Hynd, G, Lydon, KM, Palmer, MJ, Patel, M, Porcelloni, M, Richardson, J, Stenson, R, Studley, JR, Vasse, J-LCN & Winn, CL 2003, 'A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities', Journal of the American Chemical Society, vol. 125 (36), pp. 10926 - 10940. https://doi.org/10.1021/ja034606+

A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities. / Aggarwal, VK; Alonso, E; Bae, I et al.
In: Journal of the American Chemical Society, Vol. 125 (36), 09.2003, p. 10926 - 10940.

Research output: Contribution to journal › Article (Academic Journal) › peer-review

TY - JOUR

T1 - A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities

AU - Aggarwal, VK

AU - Alonso, E

AU - Bae, I

AU - Hynd, G

AU - Lydon, KM

AU - Palmer, MJ

AU - Patel, M

AU - Porcelloni, M

AU - Richardson, J

AU - Stenson, R

AU - Studley, JR

AU - Vasse, J-LCN

AU - Winn, CL

N1 - Publisher: American Chemical Society

PY - 2003/9

Y1 - 2003/9

U2 - 10.1021/ja034606+

DO - 10.1021/ja034606+

M3 - Article (Academic Journal)

SN - 1520-5126

VL - 125 (36)

SP - 10926

EP - 10940

JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

ER -

Aggarwal VK, Alonso E, Bae I, Hynd G, Lydon KM, Palmer MJ et al. A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities. Journal of the American Chemical Society. 2003 Sept;125 (36):10926 - 10940. doi: 10.1021/ja034606+