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ChemInform Abstract: Enantioselective Mukaiyama—Michael Reaction of Silyl Enol Ethers to 2‐Enoylpyridine N‐Oxides Catalyzed by Copper‐Bis (oxazoline) Complex. (2013)

George, Jimil [Verfasser] ; Reddy, Basi V. Subba [Verfasser]

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UID:

(DE-101)1280820632

Format: Online-Ressource

ISSN: 1522-2667

Content: Abstract: A variety of silyl enol ethers such as (II) undergo Michael addition with 2‐enoylpyridine N‐oxides (I) to furnish the corresponding Michael adducts (III) in high yields and enantioselectivities.

In: volume:44

In: number:30

In: year:2013

In: pages:no-no

In: extent:1

In: ChemInform, Weinheim : Wiley-VCH, 1987-2016, 44, Heft 30 (2013), no-no (gesamt 1), 1522-2667

Language: English

DOI: 10.1002/chin.201330028

URN: urn:nbn:de:101:1-2023021307374134831638

URL: https://doi.org/10.1002/chin.201330028

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2023021307374134831638

URL: https://d-nb.info/1280820632/34

URL: https://doi.org/10.1002/chin.201330028

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Enantioselective Mukaiyama–Michael Reaction of Silyl Enol Ethers to 2‐Enoylpyridine N ‐Oxides Catalyzed by Copper‐ Bis (oxazoline) Complex (2013)

George, Jimil [Verfasser] ; Reddy, Basi V. Subba [Verfasser]

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UID:

(DE-101)1279412194

Format: Online-Ressource

ISSN: 1615-4169

Content: Abstract: A catalytic enantioselective Mukaiyama–Michael reaction of 2‐enoylpyridine N‐oxides has been developed using a simple bis (oxazoline)‐copper complex. A variety of silyl enol ethers undergo smooth Michael addition with 2‐enoylpyridine N‐oxides to furnish the corresponding Michael adducts in high yields with high enantioselectivities (up to 97% ee).

In: volume:355

In: number:2‐3

In: year:2013

In: pages:383-388

In: extent:6

In: Advanced synthesis & catalysis, Weinheim : Wiley-VCH, [2001]-, 355, Heft 2‐3 (2013), 383-388 (gesamt 6), 1615-4169

Language: English

DOI: 10.1002/adsc.201200631

URN: urn:nbn:de:101:1-2023012807253297681112

URL: https://doi.org/10.1002/adsc.201200631

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2023012807253297681112

URL: https://d-nb.info/1279412194/34

URL: https://doi.org/10.1002/adsc.201200631

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ChemInform Abstract: Iron (III) Chloride as Mild and Efficient Reagent for the α‐Thiocyanation of Ketones: An Expedient Synthesis of α‐Oxo Thiocyanates. (2008)

Yadav, Jhillu S. [Verfasser] ; Reddy, Basi V. Subba [Verfasser] ; Reddy, Ummareddy V. Subba [Verfasser] ; [et al.]

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UID:

(DE-101)1295204436

Format: Online-Ressource

ISSN: 1522-2667

Content: Abstract: ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

In: volume:39

In: number:34

In: year:2008

In: pages:no-no

In: extent:1

In: ChemInform, Weinheim : Wiley-VCH, 1987-2016, 39, Heft 34 (2008), no-no (gesamt 1), 1522-2667

Language: English

DOI: 10.1002/chin.200834092

URN: urn:nbn:de:101:1-2023070706563098547674

URL: https://doi.org/10.1002/chin.200834092

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2023070706563098547674

URL: https://d-nb.info/1295204436/34

URL: https://doi.org/10.1002/chin.200834092

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Rh (III)‐Catalyzed Sequential ortho ‐C‐H Bond Annulation and Desulfonylation of 3‐Aryl‐2 H ‐benzo (e)(1,2,4) thiadiazine‐1,1‐dioxides: Access to 1‐Aminoisoquinolines (2024)

Ajay, Chidrawar [Verfasser] ; Balasubramanian, Sridhar [Verfasser] ; Subba Reddy, Basi V. [Verfasser]

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UID:

(DE-101)134671939X

Format: Online-Ressource

ISSN: 1861-471X

Content: Abstract: An efficient Rh (III)‐catalyzed C−H functionalization of 3‐aryl‐2H‐benzo[e][1,2,4]thiadiazine‐1,1‐dioxides with diaryl and dialkyl alkynes has been developed for the first time to the synthesis of 1‐aminoisoquinoline derivatives in a single step. This method involves through the formation of one C−C bond and one C−N bond followed by desulfonylation to generate a novel series of isoquinolines in good to excellent yields. This is a direct method to produce pharmaceutically more relevant scaffolds with a high functional diversity.

In: day:29

In: month:10

In: year:2024

In: extent:10

In: Chemistry, Weinheim : Wiley-VCH, [2006]-, (29.10.2024) (gesamt 10), 1861-471X

Language: English

DOI: 10.1002/asia.202400723

URN: urn:nbn:de:101:1-2410301331573.526685212588

URL: https://doi.org/10.1002/asia.202400723

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2410301331573.526685212588

URL: https://d-nb.info/134671939X/34

URL: https://doi.org/10.1002/asia.202400723

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ChemInform Abstract: Asymmetric Henry Reaction by a Chiral Cu (II) Complex: A Facile Enantioselective Synthesis of (S)‐2‐Nitro‐1‐arylethanols. (2011)

Reddy, Basi V. Subba [Verfasser] ; Reddy, Sankham Madhusudana [Verfasser] ; Manisha, Swain [Verfasser] ; [et al.]

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UID:

(DE-101)1284436322

Format: Online-Ressource

ISSN: 1522-2667

In: volume:42

In: number:39

In: year:2011

In: pages:no-no

In: extent:1

In: ChemInform, Weinheim : Wiley-VCH, 1987-2016, 42, Heft 39 (2011), no-no (gesamt 1), 1522-2667

Language: English

DOI: 10.1002/chin.201139045

URN: urn:nbn:de:101:1-2023032605541624025016

URL: https://doi.org/10.1002/chin.201139045

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2023032605541624025016

URL: https://d-nb.info/1284436322/34

URL: https://doi.org/10.1002/chin.201139045

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ChemInform Abstract: Bismuth (III) Salts as Synthetic Tools in Organic Transformations (2013)

Yadav, J. S. [Verfasser] ; Antony, Aneesh [Verfasser] ; Subba Reddy, Basi V. [Verfasser]

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UID:

(DE-101)1281105775

Format: Online-Ressource

ISSN: 1522-2667

Content: Abstract: Review: 166 refs.

In: volume:44

In: number:14

In: year:2013

In: pages:no-no

In: extent:1

In: ChemInform, Weinheim : Wiley-VCH, 1987-2016, 44, Heft 14 (2013), no-no (gesamt 1), 1522-2667

Language: English

DOI: 10.1002/chin.201314266

URN: urn:nbn:de:101:1-2023021607224344079275

URL: https://doi.org/10.1002/chin.201314266

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2023021607224344079275

URL: https://d-nb.info/1281105775/34

URL: https://doi.org/10.1002/chin.201314266

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Montmorillonite Clay-Catalyzed One-Pot Synthesis of α-Amino Phosphonates (2001)

Yadav, Jhillu S. [Mitwirkender] ; Subba Reddy, Basi V. [Mitwirkender] ; Madan, Ch. [Mitwirkender]

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UID:

(DE-101)1169051642

Format: Online-Ressource

ISSN: 1437-2096

In: volume:2001

In: number:07

In: year:2001

In: pages:1131-1133

In: Synlett, Stuttgart [u.a.] : Thieme, 1989-, 2001, Heft 07 (2001), 1131-1133, 1437-2096

Language: English

DOI: 10.1055/s-2001-15162

URN: urn:nbn:de:101:1-2018101507302998182600

URL: https://doi.org/10.1055/s-2001-15162

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2018101507302998182600

URL: https://d-nb.info/1169051642/34

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Scandium Triflate Catalyzed Allylation of Acetals and gem-Diacetates: A Facile Synthesis of Homoallyl Ethers and Acetates (2001)

Yadav, Jhillu S. [Sonstige] ; Reddy, Basi V. Subba [Sonstige] ; Srihari, P. [Sonstige]

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UID:

(DE-101)1184238472

Format: Online-Ressource

ISSN: 1437-2096

In: volume:2001

In: number:05

In: year:2001

In: pages:0673-0675

In: Synlett, Stuttgart [u.a.] : Thieme, 1989-, 2001, Heft 05 (2001), 0673-0675, 1437-2096

Language: English

DOI: 10.1055/s-2001-13379

URN: urn:nbn:de:101:1-2019042216245657920507

URL: https://doi.org/10.1055/s-2001-13379

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2019042216245657920507

URL: https://d-nb.info/1184238472/34

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ChemInform Abstract: Highly Stereoselective Synthesis of 2,3‐Unsaturated Thioglycopyranosides Employing Molecular Iodine. (2010)

Reddy, Basi V. Subba [Verfasser] ; Divyavani, Ch. [Verfasser] ; Yadav, Jhillu S. [Verfasser]

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UID:

(DE-101)1289035342

Format: Online-Ressource

ISSN: 1522-2667

Content: Abstract: The mild conditions allow high conversions in a short time and the α‐isomers are obtained as main or exclusive products.

In: volume:41

In: number:39

In: year:2010

In: pages:no-no

In: extent:1

In: ChemInform, Weinheim : Wiley-VCH, 1987-2016, 41, Heft 39 (2010), no-no (gesamt 1), 1522-2667

Language: English

DOI: 10.1002/chin.201039200

URN: urn:nbn:de:101:1-2023051105185401620196

URL: https://doi.org/10.1002/chin.201039200

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2023051105185401620196

URL: https://d-nb.info/1289035342/34

URL: https://doi.org/10.1002/chin.201039200

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Lithium Perchlorate Catalyzed Regioselective Ring Opening of Aziridines with Sodium Azide and Sodium Cyanide (2002)

Yadav, Jhillu S. [Mitwirkender] ; Subba Reddy, Basi V. [Mitwirkender] ; Parimala, G. [Mitwirkender] ; [et al.]

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UID:

(DE-101)1176466488

Format: Online-Ressource

ISSN: 1437-210X

In: volume:2002

In: number:16

In: year:2002

In: Synthesis, Stuttgart [u.a.] : Thieme, 1969-, 2002, Heft 16 (2002), 1437-210X

Language: English

DOI: 10.1055/s-2002-35216

URN: urn:nbn:de:101:1-2019012817352724193417

URL: https://doi.org/10.1055/s-2002-35216

URL: https://nbn-resolving.org/urn:nbn:de:101:1-2019012817352724193417

URL: https://d-nb.info/1176466488/34

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